FAQ

1. What is Biocell Ultravital and what is its scientific focus?
Biocell Ultravital, of Swiss origin, specializes in Cellular Renovation Therapies (CRT) designed to intervene in the fundamental biology of aging. Formulations are developed under rigorous scientific protocols using advanced biotechnology and molecular science. The active compounds are pharmaceutical-grade and naturally derived, designed to optimize cellular nutrition and function. Manufacturing is carried out under license in multiple facilities (Biocell Labs USA and authorized plants in France, Germany, and the Netherlands) and remains authorized by Biocell Ultravital Switzerland.
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2. What is Biopharmacy Mexico and what is its role?
Biopharmacy Mexico is the leading premium online store in Mexico specialized in Cellular Renovation Therapy, stem cell-based solutions, and anti-aging products. We distribute authentic, high-quality therapies designed to regenerate and optimize cellular function, repair tissues and organs, slow degenerative processes, and promote a healthier and more vibrant life.
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3. Why choose Cellular Renovation Therapies (CRT)?
CRTs address the root causes of cellular dysfunction and biochemical imbalances derived from insufficient cellular nutrition. By supplying bioactive natural compounds and derivatives from embryonic tissues, CRTs support longevity, optimize cellular metabolism, enhance regenerative pathways, and promote healthy aging at the molecular and tissue level.
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4. What are opotherapeutic extracts and why are they critical to CRT effectiveness?
Opotherapeutic extracts are biologically active preparations derived from ethically sourced ovine embryonic tissues. They contain essential proteins, growth factors, enzymes, and regenerative cofactors that support cellular function, repair, and regeneration.
• Embryonic potency: Embryonic tissues are rich in molecular signals that drive differentiation, repair, and tissue regeneration.
• Inter-species compatibility: Bioactive ovine molecules share >90% biochemical similarity with human cellular structures, enabling natural recognition and incorporation without triggering immune rejection.
• Targeted delivery: In oral therapies such as Human Ultracell VI, enteric-coated ingredients pass safely through the stomach for intestinal absorption, preserving biological activity for targeted tissue regeneration.
• Historical evidence: Opotherapy has been used in regenerative medicine for over 70 years; modern advances in purification and bioavailability have increased safety and clinical usefulness.
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5. How are the active ingredients regulated and standardized?
All biologically active materials comply with international biosafety standards and specific regulatory frameworks: guidelines from the French Agency for the Safety of Health Products (A.F.S.S.A.P.S) and European Pharmacopoeia standards for R&D and production in France and partner plants. Manufacturing facilities comply with current FDA regulations and Good Manufacturing Practices (GMP), ensuring biosafety, purity, potency, and batch-to-batch consistency.
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6. Where are the products developed and manufactured?
• R&D headquarters: Biocell Ultravital — France (main site for formula development, research, and continuous monitoring).
• European production partners: Germany and the Netherlands for specific materials and processes.
• Manufacturing in the USA: BIOCELL ULTRAVITAL USA Laboratories — modern plant for specific oral formulations and final products.
All facilities operate under standardized protocols, isolated clean-rooms, and software-controlled procedures to ensure uniform quality.
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7. What quality and safety control systems are in place?
Safety and quality are maintained at every stage:
• Continuous monitoring and follow-up to detect and prevent technical or human errors
• Software-based supervision of each production phase
• Controlled clean-room environments preserve therapeutic potency
• Active ingredients handled by trained specialists
• In-process and final product testing ensure purity and potency prior to release
• Compliance with ISO 9001, FDA GMP, and European Pharmacopoeia standards
• Pharmacovigilance and post-marketing surveillance to detect and prevent adverse reactions or incidents
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8. How is safety in therapies ensured — monitoring, prevention, and pharmacovigilance?
Biocell Ultravital’s safety discipline includes detection, evaluation, and prevention of adverse reactions and production issues. Standardized protocols and continuous analysis help prevent complications at every manufacturing stage. Active decisions are taken during production to mitigate risks, ensuring maximum safety and minimizing the likelihood of misapplication or adverse effects.
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9. What security system is used to prevent counterfeiting (anti-counterfeiting)?
To protect patients and preserve product integrity, Biocell Ultravital implemented a 4th-generation system:
• New packaging with a dual security system: tamper-evident physical tab and a QR code linked to authentication software
• Consumers can verify authenticity through the Biocell website or the free BIOCELL app (Android/iOS)
• Serialization, traceability, and controlled distribution reduce counterfeiting risks
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10. Which products enhance Cellular Renewal and how do they work?
CRTs are divided into five functional groups: Regeneration, Revitalization, Detoxification, Anti-inflammatory, and Hormonal.
Key mechanisms:
• Provide biochemical substrates, nucleic acids (DNA/RNA), enzymes, and signaling molecules that stimulate cellular renewal and metabolic reprogramming
• Oral (enteric) and injectable administration allows incorporation via endocytosis/phagocytosis and intracellular processing
• Over time (weeks), cellular effects translate into functional improvements at tissue, organ, and systemic levels, including strengthened immune function
• CRTs can be used as preventive, adjunctive, or primary therapies depending on clinical indication
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11. What clinical evidence supports CRTs and Biocell Ultravital?
More than 5,000 documented case studies have been collected by prescribing physicians worldwide. Results show preventive and complementary efficacy; over 90% of physicians report observable clinical benefits and continue prescribing these therapies.
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12. What are the documented clinical results?
Improvements in organ/tissue function, systemic revitalization, reduction of markers of disease progression (depending on context), and enhanced energy and well-being reported by patients. More than 90% of physicians indicate clinically relevant results.
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13. What are the adverse effects and contraindications?
Generally well tolerated. Contraindications include:
• Known hypersensitivity to animal proteins
• Pregnancy and breastfeeding (unless under medical supervision)
Medical evaluation is recommended before starting any therapy.
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14. How do they differ from conventional nutraceuticals?
• Pharmaceutical-grade formulations, manufactured under strict protocols and scientifically validated
• Include patented products derived from embryonic tissues with proven mechanisms of action
• Meet higher standards of manufacturing and quality control than conventional nutraceuticals
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15. Are they natural or synthetic?
All CRTs are natural, biologically sourced, without chemical additives that compromise biological activity.
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16. How is patient data privacy protected?
Biopharmacy Mexico guarantees security and confidentiality. Personal and medical information is used only for authorized clinical and operational purposes.
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17. Are they available in pharmacies?
Exclusively through certified distributors such as Biopharmacy Mexico; not sold in general pharmacies.
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18. What are the shipping policies and costs?
Biopharmacy Mexico ships only to North America (Mexico, USA, and Canada).
• Mexico: Free shipping on all orders
• USA & Canada: Free shipping with minimum purchase
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19. Are they covered by health insurance?
Not covered by health insurance.
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20. What happens with discontinued or reformulated products?
Formulas are continuously optimized; changes, discontinuations, and new launches are announced to authorized distributors and clients.
 
21. How are consultations and product recommendations handled?
Professional options:
• Paid online medical consultation: Session with a regenerative medicine specialist for personalized protocols
• Free evaluation via questionnaire: Complete the medical form or contact us by phone; our medical team evaluates and recommends suitable CRT protocols at no cost
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22. How should the products be administered?
Recommended protocols include the guidelines suggested by Biocell Ultravital. It is advised to follow a health professional’s guidance on dose, route, and duration, adapting them to each person to ensure therapy effectiveness and safety.
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23. How is quality control ensured?
ISO 9001, GMP, compliance with European Pharmacopoeia and FDA where applicable; extensive testing of active ingredients and final product.
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24. How is counterfeiting additionally prevented?
Security system with QR code and tamper-evident physical tab; verification via website or app.
Products from the Kuhravital laboratory include an additional laboratory security sticker to ensure authenticity and protection against counterfeits.
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25. Why are Cellular Renovation Therapies (CRT) an alternative to autologous stem cell treatments?
CRTs deliver sustained and safe results without the risks associated with manipulating a patient’s own cells. They represent a more affordable and practical option, with both preventive and therapeutic benefits. They stimulate regeneration and revitalization of organs and tissues through bioactive nutrients, growth factors, and compounds derived from embryonic tissues, promoting cellular renewal without invasive complications.