
Pharma Regulatory Affairs Service
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Product Specifications
Compliance Standards | FDA, WHO-GMP |
Service Areas | Multiple |
Documentation Type | Comprehensive |
Audit Types | Internal, External |
Staff Expertise | Extensive |
Usage | Pharmaceutical Regulatory support, covering quality systems, audits, documentation, and training. |
Delivery Method | On-site, Remote |
Features | Regulatory Compliance, GMP Support, Quality Systems, Documentation Aid, Vendor Audits, Staff Training |
Product Overview
Key Features
a) Quality System Certification & Documentation
b) Validation & Qualification
c) Internal Audits & Customer Audits
d) Vendor audits & Vendor qualification
e) Laboratory set up, up-gradation to FDA, WHO- GMP, USFDA, MHRA, EDQM, GLP & GMP Standards.
f) Recruitment and training.
g) Raw material, Packing material, In Process materials & Finished products specification
h) Ayurvedic formulation development & documentation as per FDA requirements.
Clients can avail this Pharma Regulatory Affairs Service at industry leading prices from us.
Company Details
Focusing on a customer-centric approach, MITCON Pharma has a pan-India presence and caters to a huge consumer base throughout the country. Get Others from MITCON Pharma at Trade India quality-assured services.
Business Type
Service Provider
Establishment
1983
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Seller Details
Pune, Maharashtra
Business Development Manager (pharma Div)
Mr. Ameya Pachhade
Address
MITCON Biopharma Centre, Agriculture college campus, Next to DIC office, Shivaji nagar, Pune, Maharashtra, 411005, India
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