Your Trusted Regulatory Partner

Medford Pharmaceuticals offers highly proficient global Regulatory Affairs services catering to all stages of Pharmaceutical, Active Pharmaceutical Ingredient (API), and other health product development and lifecycle management. We pride ourselves on being a dependable and trustworthy Regulatory Partner, committed to ensuring the smooth and compliant progression of your products in the market.

At Medford Pharmaceuticals, our workforce comprises a team of exceptionally motivated professionals, including experienced regulatory affairs (Dossier / DMF) consultants, dedicated scientists, adept trainers, accomplished doctors, and valuable industrial partners. Together, we form a cohesive unit committed to delivering top-notch services and expertise to meet all your pharmaceutical needs effectively. Our combined knowledge and passion drive us to be your ideal partner throughout the product development and regulatory journey.

INTERDISCIPLINARY TEAMS

At Medford Pharmaceuticals, we possess extensive experience in compiling, reviewing, and drafting 350 Dossiers for both semi-regulated and ROW markets. We are well-versed in handling various grades of DMFs across the globe and conducting Bioequivalence (BE) studies. Additionally, we excel in managing numerous ROW dossiers and DMFs, along with various Technical Documents like AMV, SMF, PVP-PVR, PDR, PSUR, PV, and SOP. Our commitment to delivering the highest quality services and exceptional registration dossiers has solidified our position as a trusted and reliable partner in the industry.

EXTENSIVE INTERNAL RESOURCES

Medford Pharmaceuticals operates specialized Dossier delivery teams in India, with a dedicated workforce with experienced professionals. Our facility is,equipped with state-of-the-art infrastructure for Dossier compilation and management.

IN-HOUSE DOSSIER/
DOCUMENT FACILITY