About Healthycell

As cell science revolutionizes our understanding of health & wellness, Healthycell is the health sciences company with doctors and scientists at the forefront of this movement, committed to developing the highest quality products that empower people to take control of their own health at the most fundamental cellular level. Our mission is empowering people to enhance their quality of life and healthspan by optimizing the “building block” of the body – the cell.

about-us

At Healthycell, we take pride in creating products that actually work, with formulations supported by first-class scientific and clinical evidence. First, we diligently and continuously research the existing and emerging literature to create evidence-based formulations. Second, when existing research is lacking, we fund external research projects at top tier academic research institutions in order to help develop that evidence.

Advisory Board

The Science Advisory Board provides scientific, research, statistical, medical advice and counsel to the company’s management. Healthycell is proudly supported and represented by a highly qualified set of accomplished individuals with varying skill sets and experiences that translate directly into the company’s mission.

Dr. Giampapa recently received a nomination for the Nobel Prize for his groundbreaking stem cell research, as well as the Edison Award for the Healthycell nutritional supplement for cell health. He was also awarded the A4M Science & Technology award for his development of the BioMarker Matrix Profile – the first computer program to measure aging.

Dr. Giampapa has been a keynote speaker at several international forums, most recently at the Vatican in Rome for the Second International Vatican Adult Stem Cell Conference, and the Swedish American Life Science Summit in Stockholm. He recently appeared on The Science Channel special, Stem Cell Universe with host Steven Hawking. Dr. Giampapa has been featured in various national magazines, radio and television including CNN and WABC-TV, Fox news, Geraldo Rivera, Joan Rivers, Phil Donahue, and Anderson Cooper 360.

Dr. Giampapa is published in numerous academic journals including the Annals of Plastic Surgery, the Journal of Plastic and Reconstructive Surgery, The Journal of Reconstructive Microsurgery, The Journal of Anti-Aging Medicine, and the Journal of Stem Cells and Development. He is the author of the first and only medical textbook on Anti-Aging Medicine and Age Management. He has also authored 5 books for the general public on the topic including; Breaking the Aging Code (Basic Health Publications) and The Anti-Aging Solution: 5 Simples Steps to Looking and Feeling Young (Wiley), The Gene Makeover, The 21st Century Anti-Aging Breakthrough, Quantum Longevity, and Pro-Hormone Nutrition-Optimum Aging & Maximum Health Span with Nature’s Hormone-Enhancing Nutrients, and Younger Today, coauthored with Carol Alt.

Dr. Giampapa served as a consultant for NASA for the space shuttle robotic arm. He has filed or been awarded, over 24 patents from the United States Government for unique cell culture delivery techniques, stem cell reprogramming, new drug delivery systems, and surgical instrument designs. He has been a medical consultant to Allergan Medical (NYSE: AGN), Medicis Pharmaceutical Corporation, and Sanofi-Aventus (NYSE: SNY). He also served as a consultant for stem cell applications and their use for Neostem Inc., an international biopharmaceutical company (NASDAQ: NBS).

He received his M.D. degree from Mt. Sinai Medical School in New York, New York and continued his medical training in plastic surgery at St. Lukes and Columbia Presbyterian Hospitals in NYC. Upon completion of his plastic surgery training, he completed a year of microsurgery and hand surgery at NYU Medical Center. He is a Fellow of the American College of Surgeons. Dr. Giampapa has served as Research Fellow for such other prestigious institutes as Columbia Presbyterian Medical Center in New York City and was the Director of Microsurgery and Re-plantation Surgery at the University of Medicine and Dentistry of New Jersey. He is a founding member of the American Academy of Anti-Aging Medicine, (A4M). Dr. Giampapa served as the first President of the American Board of Anti-Aging Medicine. He is also one of the first Board Certified anti-aging physicians in the world.

He continues to use his 34 years of research and surgery experience, creating stem cell technologies, especially for their applications to aging disorders, as well as cosmetic and reconstructive applications.

Dr. Neveu has over twenty-five years of exploratory research and translational development studies in both conventional and integrative healthcare. He previously served as Chief Scientific Officer for NanoSynergy where he used patented technology to improve the pharmacologic activity of nutraceuticals. Prior to this he served as President and CEO of the National Foundation of Alternative Medicine, founded by Congressman Berkley Bedell, that focused on the international identification and research evaluation of promising complementary and alternative therapies. For eight years he supervised a mechanism-based drug discovery laboratory at Pfizer that was responsible for both cancer and immunological diseases. During this period, his lab initiated novel therapeutic approaches for Tarceva™ (EGFR kinase inhibitor) and Pfizer’s first protein therapeutic, Tremelimumab™ (anti-CTLA4), that was listed on Fortune’s Top 10 list of cancer drugs. He has been an honorary fellow of the Harvard School of Public Health and the Dana Farber Cancer Institute that utilized gene expression profiling to identify several novel tumor suppressor genes (e.g. Maspin) that have been developed for the diagnosis and treatment of cancer. Mark received his Ph.D. at the University of Wisconsin-Madison McArdle Laboratory for Cancer Research, were he identified a family of Connexin genes (gap junctions) reversibly regulated by carcinogens. Mark collaborated with the Harvard Center for Risk Analysis and EPA/FDA to develop toxicology regulatory guidelines based on these findings.

He received his B.S. in Biochemistry and Nutrition from Virginia Tech, where he conducted research on the chemical synthesis of anti-cancer natural products and environmental toxicology for the State of Virginia.

Mark has published numerous highly-cited articles in leading scientific journals such as Science and Immunity and has several issued patents.

Dr. Malik M. Hasan M.D. is a Principal Owner of Monument Systems LLC. Dr. Hasan co-founded HealthTrio, LLC in 1999, and served as the President and Chief Executive Officer since March 2005. He also served as the Chairman of HealthTrio, LLC.
He has vision, expertise and years of unique experience in the fields of medicine, managed care and health care informatics.

Previously, Dr. Hasan served as the Chairman of the Board of Directors and was a Founder of Foundation Health Systems, Inc., America’s fourth largest publicly traded managed health-care company and parent company of QualMed Plans for Health (which he founded), Physician’s Health Services and Health Net, California’s largest network model HMO. Foundation Health Systems (FHS) and the predecessor company, Health Systems International, which was also founded by Dr. Hasan, has been a Fortune 500 Company since 1984. Dr. Hasan led FHS through an extraordinary period of multi-state expansion while championing an industry leading initiative, termed “fourth generation medical management“ in developing a management information system to support FHS’s physician-driven medical management approach.

As a board-certified neurologist in Pueblo, Colorado, since June 1975, Dr. Hasan maintained a limited practice until July 1992. During the 1970’s, Dr. Hasan was an advanced fellow and assistant professor of neurology at Rush-Presbyterian St. Luke’s Medical Center, Chicago. Dr. Hasan holds degrees from King Edward Medical College, Royal College of Physicians of Edinburgh and the Royal College of Physicians of London, an EMG certification from the American Association of Electromyography and Electrodiagnosis and is a Diplomate of the American Board of Psychiatry and Neurology.

From 2000 to 2003, Dr. Smith served as President & Chief Executive Officer of IP2M, a multi-platform media company specializing in healthcare. During her term, the company was selected as being one of the 10 fastest growing technology companies in Houston. IP2M was sold to a publicly-traded company in February 2003.

Previously, from 1998 to 2000, she was Executive Vice President and Chief Medical Officer for HealthHelp, Inc., a National Radiology Management company that managed 14 percent of the healthcare dollars spent by large insurance companies.

Dr. Smith has acted as a senior advisor to, and investor in, both publicly traded and privately held companies including but not limited to China Biopharmaceuticals Holdings, Inc. (“CBH”), the Madelin Fund, HC Innovations Inc., Navstar Media Holdings, Strike Force, Health Quest, Red Lion Partners and All American Pet, where she has played a significant role in restructuring and or growing the companies.

She currently serves on the Board of Trustees of the NYU Medical Center Board, is past Chairman of the Board of Directors for the New York University Hospital for Joint Diseases where she headed up new development efforts and board member recruitment, and served on the Board of Choose Living. Dr. Smith is the President and serves on the Board of Directors of The Stem for Life Foundation.

Dr. Smith received a medical degree from Yale University in 1992 and a master’s degree in business administration from the Wharton School in 1997.

Michael Nobel was born in Sweden and lived in Switzerland for many years. He is a citizen of Sweden and Switzerland. After studies in Sweden and America he obtained a doctorate at the University of Lausanne in psycho-pedagogy. The thesis subject was the evaluation of the effectiveness of substance abuse prevention programs in Switzerland. In the domain of science he worked for seven years as a researcher in social sciences at the Institute for Mass Communication at the Lausanne University and at the Department of Social Psychiatry at the Institute of Social and Preventive Medicine. He was also consultant to UNESCO in Paris and the Geneva United Nation’s Social Affairs Division in the field of drug abuse prevention.

For 15 years he represented the Nobel family as vice chairman and subsequent chairman of its board of directors. He is chairman of the Nobel Sustainable Trust Foundation in Zürich. Commercially he participated in the introduction of magnetic resonance imaging in 1980 and remained in that field for 26 years. Between 1991 and 2007 he was executive chairman of a group of companies that performed imaging services in Sweden.

Today he is chairman or board member of seven international companies in diagnostics, treatment and information systems in the field of medicine. He is also chairman or board member of five non-for-profit organizations in the field of youth education and development and peace and conflict resolution.

In the academic field Dr. Nobel was visiting professor at the Frontier Research Institute at the Tokyo Institute of Technology between 2007 and 2012. He is currently visiting professor of Kyosei studies at the Seisa University and professor at the Peace Research Institute of Soka University. From October 2015 he is appointed specialty professor at the Michael Nobel Sustainable Technology Laboratory at Osaka City University. He is a member since 2005 of the Russian Academy of Natural Sciences.

He has seven academic honor degrees including Doctor of Science HC from Soka University in Tokyo and the University of Technology in Kingston as well as Professor of Science HC from the Azeri National Academy of Science, Moscow State University, Alfred Nobel University, Russian New University and the Tambov State Technology University. Rotary International conferred on him the Paul Harris Fellowship Award in 1997 and he is honorary member of the Rotary Clubs in Karlskoga, Sweden and Miami, Florida.

In 2002 he was the recipient of the Gandhi, King, Ikeda Award from Morehouse College in Atlanta, previously given once as a shared prize to Nelson Mandela, Mikhail Gorbachev and Prince El Hassan bin Talal of Jordan.

In 2004 he became the Board of Trustees Citation awardee by the Midwest Research Institute of Kansas City. Previous laureates include Margaret Thatcher, Henry Kissinger, Paul Volcker, Edward Teller and Henry Ford. The same year he was endowed with the UNESCO medal for Outstanding Contributions to the Cultural Dialogue Between Nations.

In 2005 in Jerusalem he received the Albert Einstein Medal for Outstanding Achievements in Life Sciences and Technology, in 2006 the International Order of Perfection in Moscow and in 2010 the Gusi Peace Prize in Manila. He was awarded the Medal of Distinction by FICAC in Kingston in 2012.

In 2013 he received the Order of Duty and Honor from the United Nations Council for Public Awards and the Gold Medal from the IINC in Tambov, The World Federation of Consuls presented him its Order of Merit in 2014 in Miami. He received the keys to the cities of Hollywood, California and Florida in 2008 and the mayors of Harrisburg Pennsylvania and Miami Dade County have proclaimed official Michael Nobel Appreciation days in October and December each year.

Certifications

certificationHealthycell supplements are made in the United States only in Current Good Manufacturing Practices (cGMP)-compliant facilities, and comply with the Dietary Supplement Health and Education Act of 1994 (DSHEA).

Dietary Supplement Health and Education Act of 1994 (DSHEA):

FDA regulates both finished dietary supplement products and dietary ingredients. FDA regulates dietary supplements under a different set of regulations than those covering “conventional” foods and drug products. Under the Dietary Supplement Health and Education Act of 1994 (DSHEA):

  1. The manufacturer of a dietary supplement or dietary ingredient is responsible for ensuring that the product is safe before it is marketed.
  2. FDA is responsible for taking action against any unsafe dietary supplement product after it reaches the market.

Current Good Manufacturing Practice (cGMP):

Under FDA regulations at 21 CFR part 111, all domestic and foreign companies that manufacture, package, label or hold dietary supplement, including those involved with testing, quality control, and dietary supplement distribution in the U.S., must comply with the Dietary Supplement Current Good Manufacturing Practices (CGMPs) for quality control.

In addition, the manufacturer, packer, or distributor whose name appears on the label of a dietary supplement marketed in the United States is required to submit to FDA all serious adverse event reports associated with use of the dietary supplement in the United States. FDA’s responsibilities include product information, such as labeling, claims, package inserts, and accompanying literature. The Federal Trade Commission (FTC) regulates dietary supplement advertising.

Quality & Manufacturing

It is critical that people select a trustworthy supplement partner dedicated to quality and transparency

The Healthycell line of ingestible supplements are made in the United States at VitaQuest (supplementmanufacturers.info), a company that has built a reputation over three decades as a trusted leader in the formulation, development, and manufacture of custom dietary supplements for clients in more than 75 countries worldwide.

VitaQuest is recognized for outstanding quality with manufacturing facilities that operate under strict FDA Good Manufacturing Practices (GMP). Kosher, Halal, and organic-certified, VitaQuest has been audited and approved by leading independent bodies as well as by governmental health authorities worldwide.

VitaQuest’s quality is engineered into every product. From raw material analysis to final product inspection, every production step is carefully monitored and documented, with full accountability and in-process controls. VitaQuest’s Technical Services, Analytical, Quality Control and Quality Assurance groups offer a level of scientific support unmatched in the industry. The Quality Control/Analytical Development Department of VitaQuest consists of a highly trained staff of 17 degreed chemists under the supervision of three resident Ph.Ds., a team that performs analytical testing of raw materials, in-process samples, and finished goods in a cGMP/GLP-compliant facility.

In addition to extensive physical, chemical, and microbiological analytical capabilities, the VitaQuest Quality Group also performs the following services: (1) Stability Testing according guidelines from the International Conference on Harmonisation of Technical Requirements for Registration of Pharmaceuticals for Human Use (ICH) and customized storage conditions, (2) Method Development and Validation, (3) Technology transfer of analytical methodology.

VitaQuest utilizes a comprehensive in-house technical library, as well as online scientific databases, to review claims made by the products they produce.

Chemistry Capabilities

methodMethods Used
USP/NF, BP, AOAC, in-house, and client-supplied methods are utilized

chemical

Chemical Analysis

  • Vitamin and Dietary Supplement Assays
  • Dissolution and Disintegration according to USP and compendia procedures.
  • Elemental analysis of minerals
  • Physical Testing including Partial Size, Friability, Hardness, and Weight Variation.
  • Moisture analysis via Loss on Drying and Karl Fischer techniques
  • Identification via spectroscopy
  • Wet Chemical Analysis
  • Organic Volatile Impurities (OVI)
  • Pesticides Analysis
  • Heavy Metals Testing for various Regulatory Compliances
instrument

Instrumentation

  • HPLC/UPLC systems equipped with UV/VIS, PDA, RI, and ELSD detectors
  • UPLC/MS/MS system with ESI and APCI modes.
  • GC system with PID, FID, ECD and detection and headspace auto sampling.
  • FTIR and NIR spectroscopy systems
  • HPLC/UPLC systems equipped with UV/VIS, PDA, RI, and ELSD detectors
  • UPLC/MS/MS system with ESI and APCI modes.
  • GC system with PID, FID, ECD and detection and headspace auto sampling.
  • FTIR and NIR spectroscopy systems

Microbiology Capabilities

methodMethods Used
USP/NF, BP, AOAC, FDA-BAM, and client-supplied methods are utilized

chemical

Tests Performed

  • Microbial Limits
  • Probiotic Assays
  • Antimicrobial Effectiveness Testing (AEI)
  • Tests for Specified Organisms
  • Water and Environmental Monitoring
instrument

Instrumentation

  • Vitek automated Microbial Identification System
  • Tempo automated Microbial Assay system

Contact

87 Valley Road, Montclair, NJ 07042

[email protected]

800-975-9606

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