Your queries answered – HFMA Secretariat, CLEAR CHECK™ and advisers are at the end of a phone. You have unrestricted and free access to some of the best technical, scientific, regulatory and political advice that you could wish for. And through the HFMA you have access to our counterpart ‘sister’ trade associations in 13 other EU member states.
We are constantly fighting for the regulatory ‘rights’ for the existence of the specific ingredient forms, additives and delivery forms that our members use in their products. Our efforts in this area have been critical.
At a time when enforcement is stretched, we are keeping a level playing field, ensuring there is a way, through your trade association, to report misleading and unscrupulous competitors that could take sales/market share from you by using unfair or even illegal means. This is happening on a daily basis.
We are, on a daily basis, helping our members ensure that their products, adverts and packaging are, and REMAIN, fully compliant with all UK and EU regulations and thereby don’t fall foul of the authorities/TSOs etc.
If issues arise:
As a member you receive a constant stream of news update, ‘In the News’ and ‘Beyond the News’ bulletins, CLEAR CHECK News and other mailings, have access to an information-packed members-only section of our website, and the opportunity to attend our quarterly technical working groups meetings.
We have never been better connected to the regulatory and enforcement authorities on a national or local level. We are better connected now than ever before to the Department of Health, FSA, Regulatory Delivery, Defra, MHRA, Trading Standards Institute etc,
Through your membership of the HFMA, you can, at no additional cost, sign up to the Primary Authority Coordinated Partnership with Surrey and Buckinghamshire Trading Standards, and your being part of the PA Partnership provides you with a protective ‘shield’ that you otherwise might not have.
We spend a lot of time and effort in being on the lookout for, and handling, the media PR issuesthat always seem to be coming our way. There are countless times when we have been a voice of reason and balance in an otherwise damaging story in the national media.
It is HFMA policy to require its members to ensure that their products are manufactured according to Good Manufacturing Practice (GMP). Each HFMA member company is required, as a condition of membership, to declare that they adhere to GMP principles at relevant stages of manufacture & distribution.
A number of elements of GMP are envisaged by food legislation, particularly with respect to ‘Due Diligence’ to ensure compliance with both safety (e.g. food hygiene, prevention of contamination and other HACCP) and food information provisions (including the labelling, advertising and presentation of food supplements). For food supplements, these ‘food elements’ of GMP are required in addition to the basic principles of pharmaceutical GMP that are appropriate for the production of the dosage forms in which food supplements are usually presented.
For both general food products and food supplements, the HFMA expects all relevant legislation to be met. For food supplements, the HFMA bases its GMP standards on those included in the ‘Quality Guide for food supplements’ published by the European Federation of Associations of Health Product Manufacturers (EHPM).
The Food Supplement industry, including many HFMA member companies, is faced with ever increasing demands for proof of safety of its products and ingredients. The HFMA encourages all of its members to adopt an Adverse Event Reporting (AER) system with longer-term intention of this being a condition of membership in the future.
AER software is free to all HFMA members, and is available on request. Any questions or requests for advice on this subject should be directed to the HFMA Secretariat.