Medical

OUR SERVICES: MEDICAL & HEALTHCARE SECTOR

INMITO Consultancy services have been created with a view to provide various services viz. market research, business analysis, and viability studies for various medical and healthcare companies. Apart from this INMITI is one stop destination to all regulation and compliance information needs for various institutes.

We thrive on consistently achieving success in regulatory and marketing assignments and institutional sales, identifying potential markets and products and ensuring smooth and quick beginning of high-yielding company’s operations. Our team of consultants has expertise in channel development along the length and breath of India for Trade and Institutional Sales. Our team is also adept at providing solutions in contract manufacturing for successfully escalating business volumes & market shares and it has a good rapport with major manufacturing units having facilities of WHO-GMP standards. We are also in tie-ups with WHO-GMP Certified manufacturing units on our panel and ensure best quality products from these units. We provide tablets, capsules, liquids, liquid orals, injectables, ointments etc. including bio-technology products like infertility products, anti-cancer, anti-retroviral & anti-malarials.


BRIEF LIST OF SERVICES:
   - Company and Product Registration/ Regulatory affairs
   - Product Sourcing from India
   - Clinical Trials
   - Market studies
   - Production outsourcing
   - Market Entry strategy
   - Hospital modernization
   - Custom duty regulations
   - Organization of meetings with leading key opinion doctors
   - Organizing Seminars and conferences


REGULATORY CONSULTANCY SERVICES :
 (1) Statutory compliances.
 (2) F.D. A. licenses related to manufacturing
 (3) F. D. A. licenses related to import / export of RM, PM & finished material.
 (4) Indian agent Services for the purpose of foreign manufacturing site.
 (5) FDA licenses relating to sales of Drugs, Medicine, Devices & Diagnostics.
 (6) Compliance for GMP guideline conducting GMP inspection.
 (7) Logistics and support for statuary sampling and testing of products at various national testing centers.
 (8) Documentation for FDA, ISO- certifications, CE marking etc.
 (9) Regulation in the area of Biotechnology.
 (10) Biosafety regulations.
 (11) Regulations relating to Genetically modified organisms (GMO).