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.

#medrasm #regulatoryaffairs #pharmacist

MedRASm -(میڈراسم)

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