Welcome to TradeKey, Join Free | Sign In

or
❯
Contact Us
❯
BOOK A CALL
Book Call On Your Favorite Time

By Signing Up. I agree to TradeKey.com Terms of Use, Privacy Policy, IPR and receive emails related to our services

Get Verified Buyers & Suppliers

Avail Free Consultation

By Signing up. I agree to TradeKey.com Terms of Use, Privacy Policy, IPR and receive emails related to our services

no thanks


GLOBAL PHARMA

  • India India  
  • Last Updated:
    Posted on: 19 Nov 2024

  • Destination Port: XXX
Buyer Information

RFQ Details

Dear Sir

We provide the following services to Pharma Companies in order to make a user friendly compliance culture between various kinds of countries taking care of their in House Regulations

Development of new facility Quality Control and Quality Assurance Systems

Assisting fillings of Drug Master Files in various countries

Assisting registering products in various countries

Supporting RA, for timely completion of DMF

Assisting How to face Regulatory Audits

Assisting to file Dosage forms in various countries

Assisting Stock and Sale of API Finished Dosage forms

Assurance of all mfg Licenses, GMP WHO GMP ISO9001 ISO14001 requirements
Assisting obtaining Indian Drug License GMP WHO GMP Certificates

Assisting to get Halal Certificate from Muslim Food Board, Kosher Certificate, and AIB Certificate from American Institute of Bakeries

Effective implementation of internal as well as external Audit system at regular interval with recommendations for a consistent improvement

Organizing training programs for Production QC QA and Warehouse

Training of Quality Control Quality Assurance and Regulatory Affairs personnel according to Indian Drug Control USFDA and ICH Guidelines

Performing periodic Internal Audits to ensure that the current systems are in practice

Performing Vendor Audits for Raw Materials as third party audit evaluate and recommendation

Assisting effective use of used solvents

Assisting in preparation of Tech Packs for various customers

Assisting in Preparation of Site Master files

Preparation, periodic revision of SOP and Standard Testing Procedures for QC QA Production Maintenance, Warehouse HR departments

Equipment Qualification and validation

Process and cleaning validation

Ensuring Plant, Personnel & Equipment Hygiene and Pest Control

Monitoring & control of Good Laboratory


People who quote for this RFQ also looked at

Refine by popular tags

bulk drug bulk drug intermediates api

Recommended RFQs

Connect with us:

Copyright © 2024 TradeKey.com

Created in 0.33308 seconds