MEDIVIZ PHARMA SERVICES PRIVATE LIMITED, established in November 2013, is an organization offering a spectrum of integrated Analytical Services in Pharma and allied sectors to clients engaged in the areas of Pharma /Biotech & Environmental Sciences. Operating with ease in both national & international arenas, Mediviz provides services primarily in the following areas:
- Microbiological Analytical Services
- Regulatory Consultancy
- cGMP Consultancy
- Pre-formulations/Dossier Development
Endowed with capabilities to cartel, with a highly competent and experienced team at its disposal, Mediviz offers the best Pharmaceutical Services in the aforesaid domains. Equipped with a state-of-the-art Microbiology Testing laboratory at Visakhapatnam, Andhra Pradesh, India, conforming to the USFDA/EU GMP requirements, Mediviz ensures its clients are provided with accurate and reliable results.
Commencing with the goal of serving the Pharmaceutical companies by offering premium analytical testing services along with GMP, Auditing & Regulatory Consultancy services, Mediviz has evolved to provide microbiological services of a high order to Pharmaceutical industry.
Mr. M. Rambabu
Career Snapshot of Mr. Rambabu
- Two Decades of hardcore experience in the Pharma sector in QC, QA & RA departments.
- Rendered services as Head of the Quality Management in MNC companies.
- Proven Expertise in establishing green field sites.
- Instrumental in the submission of huge number of DMFs/CEP and Dossiers for different dosage forms all the over the world.
- Varied and relevant experience in handling all major regulatory audits like USFDA, EDQM, MHRA, TGA etc.,
Credible Regulatory Assignments
Mediviz undertakes a plethora of Regulatory Consulting assignments which range from highly regulated markets to sparsely regulated markets. As a Regulatory Consultant, Mediviz assists the clients by guiding them from the stage of product development itself; to be in conformity to that country’s specific requirements in data generation and also help in documentation for submission to various Regulatory Agencies all over the world. Mediviz processes all the queries to culminate in securing of the final approval of the concerned product, all under one roof.
Its core focus is to offer supportive services to Pharmaceutical Companies in the field of registering Pharmaceutical Dossier and admirably executes:
- Drug Master File / Dossier Writing
- DMF/ANDA / MAA Submission
- Responding to deficiencies
- Post- approval Regulatory obligations
- Preparation & Review of documentation including Bioequivalence reports and other supporting documents
- Rendering services in selection of CROs.
CDSCO & DCA (Government of India) Approved Analytical Testing Laboratory
Corporate Identity Number