PHELIXMED, based in Istanbul/Turkey, is a Regulatory Affairs Consultancy company. The regulatory affairs function within the pharmaceutical industry is vital in making high quality, safe and effective medicinal products available for patient access. We are passionate to work with you to be the success partner of your regulatory and market access procedures in Turkish pharma market. PHELIXMED, - provides full range of regulatory services covering all stages of the product life cycle; all the regulatory affairs work to receive and maintain a registration approval. - has broad experience for regulatory pathways of pharmaceuticals, biopharmaceuticals, biologicals and vaccines. Biopharmaceuticals is our particular speciality. - provides support along the GMP certification procedure, starting from the GMP certification submission to attend accompanying on-site inspection on behalf of you when needed. - provides market access services covering strategic support services for pricing, reimbursement, alternative reimbursement models, pricing&reimbursement submissions during all stages of the product life cycle. - provides support for the governmental affairs relations and follow-up procedures in Ankara where the Turkish health authority is based. - provides readability testing service - provides timely and high quality translation services with our translators who have a good command of the pharma terminology. - evaluates braille texts on mock-ups and provides expert letter on braille conformity check. Our dedicated expertise at PHELIXMED will contribute and add value throughout the process. We take the time to understand each client’s unique business objectives and operations to successfully solve problems, avoid risk and accomplish tasks correctly the first time in a genuine way. If you have any further questions about our consultancy services or would like to find out more about working with us, please get in touch via info@phelixmed.com or visit phelixmed.com.