The organic structure of women and men is different and unequal because there are
biological factors (genetic, hereditary, physiological) that manifest themselves
differently between the sexes and are often invisible to the androcentric
patterns of the health sciences. Researcher Petra Kolip, from
the Institute for Preventive Medicine at the University of
Zurich, Switzerland, considers it very important to differentiate
between biological gender, as there are gender-related differences in health and
disease. Genetic-biological differences: In men, the existence of a chromosome
(X) in his inheritance (XY) predisposes him to a greater susceptibility to
diseases, such as those that are inherited in a recessive way of the X
chromosome. In women, due to the second X chromosome (XX) slows down the aging
process. Cellular aging diseases, certain forms of cancer, and other diseases
are less common in women.
Organic Aging and Cell
Renewal Therapies
Clinical studies confirm that men and women differ in the way they get sick.
As a result of continuous research carried out by Biocell
Ultravital’s to fill the organic deficiencies of women and men
of our times, it has developed a product for each gender, mainly to optimize the
cellular structure in the Cellular Renevation stage
of women and men. In addition to containing the most efficient biocellular
compounds, it now includes biopeptides and other new components in its formulas
that are differentiated to minimize organic deterioration and the structural
needs of each genus and its implications, especially with regard to function.
endocrine, metabolic, immune and cognitive abilities.
Due to the therapeutic importance that peptides represent in the field of new
scientific discoveries, we have incorporated them to improve and enhance the
organism of 4 main activities: protection, repair, revitalization and
regeneration of all cellular functions, hence the importance of including
biopeptides to the formula Human Ultracell of a 4th cell generation.
Human-Ultracell VI, cell renewal therapy, also helps to
avoid the rate of DNA transcription errors in RNA at the time of making proteins
and DNA copying errors in the synthesis interface (S interface) prior to
Mitosis, and to reinforce the apoptosis mechanisms, to eliminate mutated or
potentially risky cells that generate the development of various diseases.
Human-Ultracell VI Cellular Renovation Therapy manages to
significantly restore the impaired functions of cells, through the supply of
extremely valuable biological components that have the ability to induce a
gradual recovery of the energy production capacity of cells and of its ability
to correctly produce the proteins necessary for the replacement and maintenance
of the body’s tissues, as well as the stimulation of cognitive faculties,
concentration, memory and mental alertness and the maximization of the potential
of the immune system.
You can improve your physical appearance, even looking younger thanks to the
magic of the plastic surgeon, we can improve our skin and surpass any marks or
expression lines, and even change the color of our hair, all to look younger,
but what can we do to rejuvenate our organs and avoid the risks of degenerative
diseases? Invest in your life, not in life insurance, invest in a future free
from disease and illness, not in hospitals and medicines.
Discover Human Ultracell VI to look young on the outside and
inside and thus be able to extend your life with health. Because “your health is
priceless”
Conclusions
Human-Ultracell VI therapy has been developed to improve the
quality of life of men and women from the age of 30 and is particularly
effective in preventing diseases, especially degenerative ones associated with
aging.
It is also highly effective as an adjunct product in conventional treatments in
the case of existing degenerative diseases.
What is Human Ultracell VI?
It is a product of biological
origin with pharmaceutical quality, considered by many specialists in
regenerative medicine as the most effective product of organic revitalization
through Cellular Renewal, which stimulates the body, especially the immune
system, to defend itself against contracting degenerative and catastrophic
diseases.
How Does it Work?
How Does it Work Human
Ultracell VI
What do we feel when we take Human Ultracell VI?
It is almost imperceptible, but it gives us the protection and security that we
feel when we have been vaccinated against contagious and viral diseases, with
the main benefit that
HUMAN ULTRACELL helps prevent organic
aging and its consequences.
What are the components of Human Ultracell VI?
It is a combination of opotherapeutic cell extracts, biopeptides, enzymes and
hormonal precursors that originate important stimuli in cells for optimal
functioning. Its formula is an exclusive worldwide patent and does not contain
chemicals, steroids, or synthetic hormone substitutes.?
What are its Benefits?
Its main benefits are:
- Slowing down the aging process.
- It prevents cell deterioration and organic wear, which are the beginning of
degenerative diseases.
- Strengthens the immune system.
- Revitalizes organs, improving their functions.
- Strengthens cognitive functions.
- Improves heart and lung function.
- Increases bone density.
- Improves the elasticity of the skin.
How does Human Ultracell Work?
It works mainly by autophagy, which is a cleaning by recycling of all the waste
inside the cells that limit key functions, decreasing their energy production
capacity in the mitochondria, therefore autophagy progressively restores the
deteriorated functions of the cells through the supply of extremely valuable
biological components that have the ability to induce a gradual recovery in the
energy production capacity of cells and the proteins necessary for the
replacement and maintenance of organic tissues.
What is the Price of Human Ultracell VI?
The price will depend on the number of doses your doctor prescribes, but this
may vary depending on the age of the patient and their health conditions. What
value do you place on your health? We must remember that the most important
thing in life is not to survive it with chronic diseases and ailments, but to
live it as long as possible fully and with health.
Do Insurance Companies cover this Treatment?
As it is a
non-pharmaceutical biological product, thus far it has not been possible to make
the necessary agreements for insurance companies to integrate this product into
their programs.
If we could Buy Insurance that guarantees Health, would we do it?
If we
reflect on the purchase of life insurance, it only gives us peace of mind, since
we have our family protected, but it does not protect our health or our future
physical well-being.
Is Human Ultracell VI available in Pharmacies?
Because it is a product of biological and non-pharmaceutical origin, it is not
for sale in traditional pharmacies, only in some specialized.
Biopharmaxie and
Schweizer Klinik Biocell
What Side Effects and Reactions does Human Ultracell VI have?
It has no side effects, since its toxicity is completely nulled, it does not
produce any adverse reaction and it can be taken safely combined with other
treatments, since it does not have any interaction with other medicines.
What are the Results of Clinical Expertise with Human Ultracell VI?
In recent years, different clinical expertise has been carried out, where it was
found that
HUMAN ULTRACELL VI also exerts a very
positive coadjuvant function in combination with other allopathic medications
and its great effectiveness as a primary treatment within the spectrum of
alternative medicine and its importance in the process of medical action in
relation to the follow-up they gave to the patient’s health.
Human Ultracell VI: Man
Longevity
Activator.
Oral presentation.
Contains 6 different formulas per dosage.
3
capsules differentiated in formulas, engraving and color of 750 mg each.
3 tablets differentiated in formulas, engraving and color of 750 mg
each
Dr. Patrick Human Ultracell
VI
Composition:
Each Enteric Coated White Tablet 750 mg contains:
Opotherapeutic Extracts: Umbilical cord, Embryo, Placenta, Thymus,
Mesenchyme, Muscle, Testicles.
Peptide Extracts: Umbilical Cord, Embryo, Placenta, Thymus, Mesenchyme,
Muscle, Testicles.
Other Assets: Adénine Diphospirine Dinucléotide (NAD),
Trans-Resveratrol 3-4-5, Superoxide Dismutase, Glutathione Peroxidase,
Glutathione Reductase, Glutathione Transferase, Adenosine Triphosphate (ATP),
Vitamin B1 Complex, Vitamin A, Potassium gluconate, Osteol, Vinpocetine,
Pregnenolone, stabilizers and excipients.
Composition:
Each enteric-coated 750 mg Red Tablet contains:
Opotherapeutic Extracts: Umbilical cord, Embryo, Placenta, Thymus,
Heart, Lung, Prostate.
Peptide Extracts: Umbilical cord, Embryo, Placenta, Thymus, Heart,
Lung, Prostate.
Other Assets: Adénine Diphospirine Dinucléotide (NAD),
Trans-Resveratrol 3-4-5, Vinpocetine, Pregnenolone, Lycopene, Hydroxytyrosol,
Vitamin B9, Vitamin H, Copper Gluconate, Lapacho, Exocyan, Adenosine
triphosphate (ATP) Superoxide Dismutase, Glutathione Peroxidase, Glutathione
Reductase, Glutathione Transferase, stabilizers and excipients.
Composition:
Gray Tablet 750 mg enteric coated contains:
Opotherapeutic Extracts: Umbilical Cord, Embryo, Thymus Placenta,
Liver, Pancreas, Testicles.
Peptide Extracts: Umbilical Cord, Embryo, Placenta, Thymus, Liver,
Pancreas, Testicles.
Other Assets: Adénine Diphospirine Dinucléotide (NAD),
Trans-Resveratrol 3-4-5, Vitamin B12, Calcium Phosphate, Manganese Gluconate,
Vinoserae, Zinc Gluconate, Adenosine Triphosphate (ATP), Vinpocetine ,
Pregnenolone, Superoxide Dismutase, Glutathione Peroxidase, Glutathione
Reductase, Glutathione Transferase, stabilizers and excipients.
Composition:
Gray Capsule 750 mg contains:
Opotherapeutic Extracts: Umbilical Cord, Embryo, Placenta, Thymus,
Bones, Adrenal, Prostate.
Peptide Extracts: Umbilical Cord, Embryo, Thymus, Placenta, Bones,
Adrenal, Prostate.
Other Assets: Adénine Diphospirine Dinucléotide (NAD),
Trans-Resveratrol 3-4-5, Vitamin C, Vitamin E, Magnesium Gluconate, Adenosine
Triphosphate (ATP), Riboflavin, Thiamine, Isonicotinate, Hypericin, Superoxide
Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione
Transferase, stabilizers and excipients.
Composition:
Red Capsule 750 mg contains:
Opotherapeutic Extracts: Umbilical Cord, Embryo, Thymus, Placenta,
Kidney, Testicles.
Peptide Extracts: Umbilical Cord, Embryo, Thymus, Placenta, Ovary,
Kidney.
Other Assets: Adénine Diphospirine Dinucléotide (NAD),
Trans-Resveratrol 3-4-5, Vitamin C, Vitamin B5, Ferric Gluconate, Ginseng,
Vinitrox, Vinoseed, Adenosine Triphosphate (ATP), Riboflavin, Thiamine ,
Isonicotinate, Hypericin, Superoxide Dismutase, Glutathione Peroxidase,
Glutathione Reductase, Glutathione Transferase, stabilizers and excipients.
Composition:
750 mg Red / Gray Capsule contains:
Opotherapeutic Extracts: Umbilical Cord, Embryo, Thymus, Placenta,
Brain, Prostate.
Peptide Extracts: Umbilical Cord, Embryo, Thymus, Placenta, Uterus,
Brain.
Other Assets: Adénine Diphospirine Dinucléotide (NAD),
Trans-Resveratrol 3-4-5, Vitamin B6, Vitamin B2, Zinc Gluconate, Adenosine
Triphosphate (ATP), Riboflavin, Thiamine, Isonicotinate, Hypericin, Superoxide
Dismutase, Glutathione Peroxidase, Glutathione Reductase, Glutathione
Transferase, stabilizers and excipients.
Indications:
- Regeneration, revitalization and cell renewal for human longevity, through
the reinforcement of the immune system.
- Adjuvant in degenerative diseases of the immune system.
- Premature aging.
- Decreased mental and physical faculties, fatigue, physical asthenia.
- Prevention of degenerative diseases.
- General energy increase.
- Revitalization of bodily functions.
- Increased resistance to stress.
- Improved performance and organic function that weakens with aging.
- Remarkable improvement in physical performance.
- Improved blood pressure.
- Recovery of concentration and memory capacity.
- Improved quality of sleep.
- Prevention of osteoporosis.
- Stimulation and control of libido in men and women.
- Strengthening of the venous system, acceleration of wound recovery.
- Stimulation of endogenous production of growth hormone that maintains muscle
mass.
- Prevention of senescence keeping the patient as a young adult.
Mechanism of action
The
Human Ultracell
VI formula contains cellular and phytochemical biological
compounds, which are administered to the patient orally or intramuscularly, and
once in the body are transported to the bloodstream reaching the blood
capillaries and from there to the extracellular matrix. The extracellular matrix
is a network of molecules, proteins and carbohydrates that are arranged in the
intercellular space and that are synthesized and secreted by the cells
themselves. From the extracellular matrix the components of the formula pass
into the cells, through the cellular means available for it, mainly endocytosis.
Human-Ultracell VI contains a large number of cellular
components, embryonic growth factors, nucleotides and cytokines, which require
massive incorporation into the cell. In this massive incorporation,
extracellular molecules can enter the vesicle nonspecifically, in solution, or
specifically bound to membrane receptors, termed endocytosis and pinocytosis.
Endocytosis consists of a transport medium according to which the cell forms a
depression in its membrane, which engulfs the elements to be incorporated,
forming a vacuole that then closes around these elements and transports them to
assimilation and digestion bags called Lysosomes, where they are catabolized and
assimilated.
Pinocytosis is a type of nonspecific endocytosis of dissolved molecules. Some of
the contents of any vesicle that forms on the plasma membrane will have
dissolved molecules that have seeped into the vesicle in a non-specific manner.
To a greater or lesser extent, all endocytosis routes carry out pinocytosis.
Cycles of the Mechanism of Action
The cell renewal process occurs
continuously and its efficiency depends on the physiological state or
physiological age of the patient, in other words on their degree of
deterioration. Although we cannot speak of defined stages of therapy action, we
can use the concept of cycles to define the sequence of its renewal processes.
CYCLE 1
CELL REVITALIZATION: The high content of coenzymes NAD
(Nicotinamide Adenine Dinucleotide) of the formula, essential for the efficient
production of energy of the cell, in the phase of Oxidative Phosphorylation,
together with the inducers of proliferation of mitochondria of the formula,
almost immediately contribute to increasing the production of cellular energy,
which allows cells to develop a process of AUTOPHAGY, cell cleaning, to get rid
of denatured proteins and other useless biological material, accumulated in
their cytoplasm as a result of poor functioning cell functions over time. Said
biological material is digested in lysosomes, or vesicles of digestion by
hydrolase enzymes, to be reused in the production of new proteins for the body.
Cells freed from the overwhelming burden of biological waste, and with increased
energy production, undergo a great revitalization. It is important to note that
AUTOPHAGY takes on special significance in the case of cells that do not divide,
such as neuronal and cardiac cells, and those that divide little, reducing the
risk of accumulation of harmful proteins that hinder their functions. It is
worth mentioning that Alzheimer’s disease is associated with the accumulation of
amyloid proteins in neurons. It has recently been discovered that the coenzymes
NAD are not only essential for the efficient production of cellular energy,
adenosine triphosphate (ATP), but also that they are key for efficient
intracellular communication in the chronological execution of their functions,
hence a decrease in its amount in cells, contributes to aging.
CYCLE 2
CELL RENEWAL: With the progressive recovery of the
energy production capacity induced by the formula and by the effects of the
growth factor stimulating cytokines in the formula, a process of normalization
of cellular functions begins, particularly its machinery for the production of
membrane proteins and lipids. In this cycle, the controls in the transcription
of DNA into messenger RNA and translation into proteins are also reinforced, to
avoid errors in the amino acid sequence of said proteins. In addition, the
semi-conservative replication mechanisms of DNA are reinforced, prior to mitosis
at the cellular interface and the cellular capacity to correct copying errors.
In addition, cells improve their protection mechanisms against mutations,
reinforcing their capacity for apoptosis of mutated cells.
CYCLE 3
ORGANIC RECOVERY: The normalization of cellular functions
leads to a greater production of proteins, which translates into an increase in
muscle mass, an increase in collagen in the skin, joints, connective tissue,
improvement of liver, kidney, and lung function, cardiovascular, in addition to
cognitive functions, memory, ability to concentrate, etc. and stimulates the
immune system. The synergistic action of the amino acids and catalyst peptides
of Human Ultracell induces and stimulates the pituitary gland to release a
greater proportion of human growth hormone (whose production decreases
appreciably with age), which acts directly on all tissues of the body, causing
the activation of a younger metabolism, characterized by an increase in protein
synthesis in almost all cells of the body, increased mobilization of fatty acids
from adipose tissue, increased amount of free fatty acids in the blood and
preferential use of fatty acids as an energy source instead of glucose. This
cycle almost always begins in week 3 or 4 and reaches its peak within 6 months.
Administration:
Orally, consume before taking food to improve absorption, preferably with water
in the morning.
Dosage:
Corresponds to 4500 mg for each daily dose consisting of the contents of 1 vial
containing 6 pills (capsules and/or tablets) of 750 mg each. Each pill is
specially formulated for prolonged release to withstand digestive enzymes
facilitating absorption in the small intestine. Daily doses are provided in the
contents of individual vials intended to be taken daily. We recommend the
contents of each vial be taken once opened within that day. The packaging is
comprised of 3 cycles containing 5 daily doses each (15 vials total). Treatment
should be implemented in the following nature Cycle 1 for 5 days taking contents
of 1 vial daily (six pills). Cycle 1 should be followed by Cycle 2 for 5 days
consuming the contents of 1 vial daily. Cycle 2 should be followed by Cycle 3
for 5 days consuming contents of one vial daily. This 15-day regiment should be
repeated for another 15 days in the same manner to complete a 30 day monthly
recommended treatment. This dosing should be completed without intervals or
interruption. Follow up dosing should be implemented according to patient’s age
and doctor recommendation.
Human Ultracell Oral Protocol:
Depending on the condition and age, the dosage orientation varies to optimize
the effectiveness of the treatment.
Indications for taking the product.
Posology 1 Preventive Therapy.
As preventive therapy in asymptomatic patients to prevent degenerative diseases
and slow down aging.
Frequency and dose by age.
From 30 to 39 years 30 doses and repeat every 6 months. *
From 40 to 49 years 30 doses and repeat every 4 months. *
From 50 to 59 years 30 doses and repeat every 3 months. *
After 60 years, 30 doses and repeat every 2 months. *
* Each dose corresponds to one dose per day.
* Restart annually for equal periods according to age.
IMPORTANT:
Do not interrupt the recommended doses of treatment, its therapeutic effect is
of continuous action, its effectiveness will depend on the completion of the
treatment.
Posology 2 Clinical Treatment.
As Adjuvant Therapy for symptomatic
patients suffering from a disorder or disease, or people with a marked family
genetic inheritance to contract diseases.
Frequency and dose by age.
From 30 to 39 years 45 doses every 6 months.
*
From 40 to 49 years 45 doses every 4 months. *
From 50 to 59 years 45 doses every 3 months. *
After 61 years 45 doses every 2 months. *
* Each dose corresponds to one dose per day.
* Restart dose cycles for equal periods annually.
Chronic diseases it is recommended to consult a doctor for the corresponding
indication.
IMPORTANT:
Do not interrupt the recommended doses, its therapeutic effect is of continuous
action, its effectiveness will depend on the continuity of the treatment.
Side effects:
Due to its peptide and opotherapeutic content in its formula, it could in some
cases cause a slight headache, which disappears after a few minutes, nausea is
very occasional and disappears in a few hours.
Contraindication
It can be safely combined with other medications.
In the recommended doses, no adverse reactions have been observed in any case.
Presentation and packaging:
Contains 45 enteric-coated tablets and 45
enteric-coated capsules with engraving and different colors that are packaged in
15 sterile vials with stoppers and security seal with the printed name of the
brand on tear-off to preserve quality of each of its different formulas and
presentations.
Extraction and obtaining of biopeptides and cellular extracts
It should
be noted that the formulas contain biological components of animal origin in
combination with other compounds that enhance the therapeutic action and are
extracted especially in the embryonic stage and processed during the second
month of gestation, these components that are part of the formulas of some of
Our products are obtained after a long biochemical process and are certified
free of prions, pyrogens, bacteria, nano-bacteria, fungi, viruses and after many
controls, the risks of an immune reaction in Humans are 100% eliminated.
Many years of clinical experience has shown that pigs and sheep are the best
donors, because they are strong and immunologically resistant. Proof of this is
that even in the 21st century, most heart valve transplants for humans are
derived from pigs, in addition to insulin and many derived products for
therapeutic purposes, come from these. These methods are continuously monitored
to determine that they meet the strictest standards required by biosafety for
therapeutic purposes. All the components and other active ingredients of the
formulas are also approved by the Federal Food and Drug Agency
(FDA) and are manufactured in the USA by BIOCELL
ULTRAVITAL USA under Swiss license from Biocell
Ultravital.
Conservation:
Keep in a dry and cool place at room temperature between 5
° C and 40 ° C. Do not use after the expiration date, nor when the present vial
has broken the safety cap, nor when the outer packaging is open or forced.
Control of finished product:
Two (2) independent laboratories perform various tests and mycotic controls,
biological, bacteriological type 5 analyzes, multicenter immunocellular tests,
Anti brucellosis, Virological controls, multiple anti-prion tests, Bacteriosis,
Cyclospores, Mycobacteria, Salmonellosis in accordance with the subject of
biology for therapeutic purposes for human consumption according to current EC
regulations
Warning:
Biocell Ultravital guarantees the purity and quality of
its products and is not responsible for damage to third parties that may cause
malpractice.
How Does it Work?
How the Formulas are Developed?
All our products have been formulated to
optimize cell function because if we have healthy cells, we will be healthier
every day, and they are based on our 4 pillars of cellular longevity. They work
together as a whole to promote energy production and cell growth.
We strive to achieve perfection for each of our therapeutic categories, since
they are formulated by carefully selecting each component after confirming its
characteristics and clinical trials that positively compromise the efficacy in
each formula, this is basically the science on which our products and therapies
are based.
Biocell Ultravital
products are formulated with ingredients that
are 100% natural biological substances, with the highest quality standards,
containing cellular extracts of animal origin and peptide hydrolysates extracted
from plant extracts and glands of young animals in combination with
antioxidants, enzymes and vitamins we managed to optimize the formulas and their
therapeutic scope.
All raw material sources are carefully selected from organic plants and organs of
pigs and sheep less than one year old and undergo
a prion and decontaminated pharmaceutical
standardization process that meets high biosecurity standards for reach specific
concentrations of high purity and are processed under strict controls to
guarantee the high quality and purity of their products.
No chemicals, other harmful or unwanted substances are used in the extraction.
Modern technology ensures the recovery of assets in a biologically natural way,
without changes. This is very important for the safety of each formula. None of
the components in Biocell Ultravital formulas are
genetically modified. (NON GMO)
Production and Extraction of Bio Peptides 4th Cellular Generation
The
chemical synthesis to produce bioactive peptides of the 4th cell generation of
Biocell Ultravital are obtained using combined methods of
enzymatic hydrolysis through proteolytic enzymes and by fermentation using
starter cultures. This combination of both methods gives origin to peptides with
a safer biological activity due to the fact that in one all the contaminating
traces are eliminated and the other facilitates the absorption through the
intestinal tract. An additional advantage of enzymatic hydrolysis is the
reduction of allergens. The procedure to obtain, isolate and identify
biopeptides with specific biological activity, is obtained with the solution of
the gland or organ to extract biopeptides, to which papain, pepsin, trypsin are
added, the application of different enzymes pursue the formation of a mixture
with different ranges of biological activity and incubated for a certain time to
obtain the desired degree of hydrolysis.
After this, the hydrolyzate is fractionated by exclusion chromatography and
semi-preparative liquid chromatography in reverse phase, selecting the fraction
with the highest activity as a result of the first invitro tests, and finally
the sequence of the peptides responsible for generating the activity is
identified. The desired therapy is obtained by applying mass spectrometry and /
or N-terminal sequencing. However, hydrolysates are complex mixtures and can
contain up to hundreds of different molecules, therefore, locating bioactive
peptides in these procedures is a biochemical work of constant expertise that
results in a difficult task and requires a lot of time and dedication. The
fractions usually still contain multiple compounds that require additional
cycles of fractionation, concentration and evaluation of bioactivity to be able
to identify the molecule responsible for the activity in the formulas of each
product according to the therapeutic indication.
Consequently, the enzymatic hydrolysis used offers undoubted advantages, such as
the absence of substrate degradation processes since the enzymes are selective
for a type of bond, pH values between 5 to 10 and the temperatures
between 40 to 60ºC, thus maintaining or improving the nutritional value of the
protein. The specificity of the enzyme affects the size, quantity, and
composition of free peptides and amino acids, as well as their amino acid
sequence.
Safety in Therapies
Safety control is a very important factor,
especially when it comes to high quality health products, which is why
at
Biocell Ultravital in France, which is the main
headquarters where all the research and development of the formulas take place,
we have monitoring and follow-up mechanisms for each product, this to prevent
any error in the next production, that is why we are continuously implementing
software for the detection of technical failures of the human team in charge of
production. This translates into maximum safety controls that guarantee the
complete quality of the production, eliminating 100% possible adverse reactions
due to the indication of some of our products that does not correspond to a
contraindication already described.
This discipline has become responsible for quality control in the formulation and
manufacturing phases thanks to the detection, evaluation, knowledge and analysis
for the prevention of adverse reactions and other possible problems related to
the products, covering a wide spectrum of continuous analysis so that they do
not cause any harm to the patient. We actively participate in
decision-making when manufacturing to prevent possible complications in any of
the production stages. Thanks to the standardization and development of specific
protocols established for each production and subjected to continuous analysis
adhering to very specific guidelines we are able to prevent these unwanted
complications. We are mandated by compliance with the European Pharmacopoeia in
Europe and adhere to current FDA regulations when manufacturing the different
products corresponding to Biocell Ultravital Cellular Renovation
Therapies.
Research and Development
When
Biocell
Ultravital incorporates products with new formulas and they
reach the market, at least an average of 5 to 7 years have elapsed, consumed in
the different phases of research and development. This journey requires a
scientific and economic effort, for this reason we say that out of every 300 new
formulas that are beginning to be investigated, only 20 end up becoming
treatments available to patients either as an adjunct or preventive of cellular
function and the immune system.
Working in the context of formulas based on opotherapeutic extracts or cells of
xenogeneic origin, they aim to support the expansion of products for basically
strengthening the immune system.
Cellular Renovation Therapy may contribute as reinforcement
to the primary treatment to treat the various human diseases that are associated
with failures of the immune system. In order to achieve this purpose the
continuous efforts of a scientific committee structured by various institutions
in the field biology headed by Prof. Dr. Ben L
Pfizer is needed. These contributions guide new formulations
that improve the components has been allocated to four fundamental guidelines
with specific objectives corresponding to the 4th generation
cellular products by Biocell Ultravital: Protection, Repair, Revitalization
and Regeneration properties. These therapeutic lines are
developed with a common research and development strategic plan for each product
category.
Manufacturing Plants and Procedures
In Europe, research, production and development is carried out
at Biocell Ultravital, France, and we share part of the
manufacturing in two other associated plants, mainly for the production of some
raw materials, between Germany and the Netherlands.
We also manufacture our products in the USA, BIOCELL ULTRAVITAL USA
Laboratories, where we have a modern production factory especially
for manufacturing formulas and products for oral presentation.
Since our products formulas require components be extracted from a biological
source, in all manufacturing plants we have ensured that they are manufactured
in production rooms that have state-of-the-art equipment controlled by software
that manages the procedures monitoring each phase of the process. Development
with the latest air conditioning, quality and safety systems, to ensure that the
final product does not lose its therapeutic potency, for this reason the active
ingredients of each formula and the preparation in the initial phase are
conditioned in isolated clean rooms and by specialized professionals trained to
measure and control the production process from the moment this first
manufacturing phase begins and continuing these quality controls through each
phase of production until the final product is approved.
Each manufacturing plant, although with different facilities, produces with the
same manufacturing procedures, efficiently following the highest quality
standards that comply with all the regulations established by
the European Pharmacopoeia and
the FDA.
Products that Improve Cellular Renovation
Currently there is a growing
interest in cell therapy extracted from the patient’s own stem cells, unlike our
products,
Cellular renovation therapies (CRT) provide
sustained results without complications and represent a great economic saving in
comparison. The products in the Biocell Ultravital line of
Cell
Renewal Therapies are divided into 5 main groups that include:
Regeneration, Revitalization, Detoxification, De-inflammatory and
Hormonal.
CRT have worked with great success in recent years as
a preventive treatment, without discarding its effective action as a primary
therapeutic. The treatment benefits are notorious for their adjuvant action in
allopathic medicine. CRT, through their formulas,
exclusively allow us to transform diseased or aging organs into healthy organs
with a highly functional capacity. Their components activate a series of
stimuli that cells need for a normal cycle of continuous renewal, and they can
be incorporated into the body through injections or orally. These various
components are assimilated by the body through endocytosis and a good part is
introduced into the cells. This is produced by the emission of pseudopods until
they completely encompass it to form a vacuole, which then fuses with the
lysosomes to degrade the phagocytosed substance, which is known by the name of
phagosome. This method is characterized by being the mode of nutrition used by
cells through ingestion of foreign matter. In addition, it is one of the greater
means of transport that they use to defend themselves against some cells of
multicellular organisms.
From this mechanism and many other stimulating biochemical changes, nutrition
begins for an effective CELLULAR RENOVATION.
CRT brings a fresh genetic information contained in DNA
and RNA, stimulating secretion inducing old or sick cells and reprogramming to
operate properly, providing the recipient bodies, a large number of biochemical
and enzyme substrates containing information needed to revitalize an organ, or a
gland. CRT contains various compounds that are
primarily responsible for properly nourishing cells, but, moreover, each of the
formulas in a CRT contains cells and embryonal
tissues that increase positive changes in cell cycle complementing in part
dysfunctional lapses. This is how the different components are first
incorporated as essential nutrients and as well, how the embryonic tissues reach
the organ with low vitality and that need to be dynamized. This process is
called CELLULAR RENOVATION and its benefits are
perceived after several weeks, as it passes slowly from the cell to the tissue,
from the tissue to the organ and from the organ to the system. Some specialists
feel that the most important result of using CRT is
the revitalization of the body’s immune defense mechanisms. When damage occurs
to the cells that make up the different tissues and organs involved in the
immune system, either through aging or environmental poisoning, the body becomes
defenseless from both external invasion and internal degeneration. The damage
caused to the organs of the immune system can be reversed by stimulating the
body’s defense mechanisms to boost the health of the weakened organ.
Security System to Prevent Falsification
Biocell
Ultravital has developed for the
4th
generation a sophisticated security system for its products to
prevent the repetition of copies and / or counterfeiting of our products. Moving
forward, we will invest a great technological effort in each package to ensure
that you will have an original product in your hand.
This security system is applied to new packaging that have a QR Scan code applied
to a double security system, a first physical stage in the packaging that will
reveal through a security tab if the product has been violated and a second with
an implantation of sophisticated software that will allow you to check if the
product you purchased is original through our website, or by downloading the
new BIOCELL APP for Android and IOS for free.
The falsification of ethical and health products is a problem that is becoming
increasingly important, and all the different therapeutic areas may be affected.
These counterfeits seek to pass for authentic products, copying the packaging
material, the commercial image, the logo, the information brochures, as well as
the shape and colors of the original product.
In addition, they use the same lot number, expiration date and other identifying
elements of the authentic product. However, they are manufactured and placed on
the market without the authorization of any health authority. These original and
generic medicines, as well as vitamins are also falsified and even more so those
products that enjoy prestige are the most vulnerable and these falsifications
may contain active ingredients in incorrect doses or lower doses than those
authorized, or the absence of active ingredients and even include some toxic
elements. Many may even be manufactured under dangerous conditions that are not
controlled. Thus, they can pose a significant risk to health and are sometimes
especially difficult to identify.
In short, they look identical to the original product, but contain “uncontrolled”
components that are life threatening.
he trade in counterfeit medicines is controlled by international criminal
networks, and no region is exempt. Those countries with less controlled drug
distribution systems are more vulnerable to this type of practice; However, the
most developed countries are not spared from this evil, especially when patients
purchase drugs on the internet or unauthorized websites. Unfortunately, in the
past we have been victims of these unethical organizations and have had to
report these facts to the authorities since many people especially in Asian
countries, as well as Mexico and others in Central and South America are victims
of misleading offers of therapies, even by unethical doctors who offer the
products at prices lower than the real cost. However, in the end they spend more
money due to the need to seek immediate clinical help as demonstrated on several
occasions reported by us through our attorneys around the world from patients
who were treated clinically for administering fake products.
