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Exclusive to AAHP Members is this annual briefing on the latest legal and regulatory issues from AAHP Legal Counselor Al Lorman, Esq. and on federal programs affecting your business from AAHP Lobbyist Pete Evich of Van Scoyoc Associates.Find out more »
Be prepared for the upcoming February 2022 submission deadline as well as the subsequent reporting deadline in May 2022. The AAHP brings you a 30-minute webinar to get your company well on its way to fulfilling this task with a minimum of pain and effort.Find out more »
EAS GMP Compliance Seminar cGMPs - Important Considerations of HPUS and CFR Homeopathic manufacturing sites ranked lowest on FDA's 2019 Site Inspection Scores (SIS). Our industry was rated at 6.5 versus an average across all application types of 7.4. Although the score was affected by many first-time inspections, the industry has work to do. Learn directly from two former FDA inspectors during this four-hour cGMP seminar. The event will help homeopathic manufacturers prepare for FDA enforcement by facilitating an understanding…Find out more »
Exclusive to AAHP Members is this semiannual briefing on the latest legal and regulatory issues from AAHP Legal Counselor Al Lorman, Esq. and on federal programs affecting your business from AAHP Lobbyist Pete Evich of Van Scoyoc Associates. Emerging issues and critical topics will be addressed as necessary. Additionally, AAHP officers will provide updates on association projects. AAHP Members are encouraged to invite your government affairs team, quality assurance team, marketing team, R&D team, and CEO.Find out more »
IN PERSON AT EXPO! Join us for this complimentary and in-person event at the historic Union League of Philadelphia, or view it virtually. Just a 5-block walk from Natural Products Expo East and a 10-minute cab ride from Amtrak’s 30th Street Station.Find out more »
Does your company experience a gap between 21 CFR cGMP requirements and the pragmatic realities of implementation for homeopathic drug products? AAHP, in partnership with the Homeopathic Pharmacopoeia Convention of the United States (HPCUS), has identified five technical gaps that are challenges for both industry and FDA inspectors. In a continuation of this industrywide, multi-year effort, the 2021 Summit will present:
• Concept Paper: Process Validation for Preparation of Hahnemannian Liquids
• White Paper: Control of Active Pharmaceutical Ingredients
• Views on these pharmaceutical quality issues and necessary compliance considerations by Richard Lostritto, PhD, Associate Director for Science, Office of Policy for Pharmaceutical Quality at FDA’s CDER.
This half-hour webinar will review additions and changes to monographs in the Homeopathic Pharmacopeia of the United States (HPUS), including revised attenuation levels, and updates to quality control methods and specifications. HPUS insider Eric Foxman provides a fresh glimpse a month after the HPCUS annual meeting on year-long projects being done behind-the-scenes and the status of the “technical gaps” work. Whether you manufacture or just market homeopathic drug products, the changed information in the HPUS has a bearing on your products’ compliance status. Regulatory and FDA review of homeopathic products over the past year support the critical importance of being current with the updates in the HPUS. These changes and updates may affect your business, your cGMP compliance, your products, and your long-term success in the market!Find out more »
Hear from the world’s leading researcher Rachel Roberts, BSc(Hons) MCH RSHom FSHom FFHom(Hon)
Chief Executive at London’s Homeopathy Research Institute.
Join us for The American Association for Homeopathic Medicine's Annual Membership MeetingFind out more »
Poison Control in 2021: A Complimentary Informational Webinar for Homeopathic Product Safety Stakeholders
Join us to learn about Poison Control Center reports of exposure to homeopathic drug products, and how you can work with the National Capital Poison Center (NCPC).Find out more »