Janet Ellis
Regulatory Affairs Director
"I've handled the regulatory affairs of products from the biotechnology, pharmaceutical and complementary therapy industries including vaccines, novel dosage forms, generics, OTC products, herbal and homeopathic medicines, food supplements and borderline products.
I've project managed a wide range of submissions including EU mutual recognition, centralised and national marketing authorisation applications, clinical trial applications and submissions to Ethics Committees and has handled applications to regulatory authorities in Europe, The Middle and Far East, South America, Asia and Australasia."
Janet has a background as a pharmacist, with a PhD in pharmaceutical microbiology from the University of Nottingham.
Do you currently market or plan to launch new Cosmetic Products in Europe?
If you are planning to launch a new cosmetic product in the EU or would like to update existing dossiers, PDS can help. Our team of experts will help you prepare for new EU Cosmetic Regulations.
PDS can prepare or update your entire cosmetic dossier or help you with the following activities necessary to market cosmetics in EU:
• Prepare cosmetic dossier or update sections of dossier
• Qualify ingredient raw materials in cosmetic formulation and intended use
• Check compliance of ingredients
• Prepare toxicology safety assessment
• Advise on label requirements
• Review claims and prepare justification of effects claimed
• Write cosmetic standard letters
• Advise on borderline product issues
Prepare cosmetic dossier or update sections of dossier
Qualify ingredient raw materials in cosmetic formulation and
intended use
Check compliance of ingredients
Prepare toxicology safety assessment
Advise on label requirements
Review claims and prepare justification of
effects claimed
Write cosmetic standard letters
Advise on borderline product issues
