MedRASm -(میڈراسم)

We offer services like CTD, eCTD file preparation, CTD Compilation, ACTD Compilation, Medical devices, Cosmetics, Consumer Division/Personal care, Supplements, Veterinary, Herbal products & Toys with authorities throughout the Globe. We are Contract Research Organization (CRO) that provides integrated services and consultancy to Pharmaceuticals, Nutraceuticals, Herbal, Cosmetics/Consumer Division, Biotechnology and Medical devices companies. Regulatory professionals are responsible for: Keeping track of the ever-changing legislation in all the regions in which a company wishes to distribute its products. - Advising on legal and scientific restraints and requirements. - Collecting, collating and evaluating scientific data. Presenting registration documents to regulatory agencies and carrying out any subsequent negotiations necessary to obtain or maintain marketing . authorization for the products concerned. Giving strategic and technical advice at the highest level in their companies, making an important contribution both commercially and scientifically to the success of a development program and the company as a whole helping the company avoid problems caused by badly kept records, inappropriate scientific thinking or poor presentation of data. Website https://www.medrasm.com/ Phone (& WhatsApp) +92-335-9000-267 Company size 2-10 employees Includes members with current employer listed as Regulatory Affairs, including part-time roles (remote). Founded: 2018 Specialties ACTD Dossier, Herbal & Nutraceuticals Dossier , eCTD Dossier, CTD DOSSIER, Regulatory affairs, Cosmetic Dossier, Food Supplements, Drug Regulatory Affairs, DMF, Drug Master Files, CIS countries, Asian Countries, African Countries, Third party manufacturing, Tablets , Capsules, Lozenges, Injections, sachets, Soft gel Capsules and other dosage forms. Hashtags: #medrasm #regulatoryaffairs #pharmacist