India
Audits, Indenting, Trading of natural products, bulk drug intermediates order in Baddi
Currency INR
Audits, Indenting, Trading of natural products, bulk drug intermediates order in Baddi
Order Audits, Indenting, Trading of natural products, bulk drug intermediates
Audits, Indenting, Trading of natural products, bulk drug intermediates

Audits, Indenting, Trading of natural products, bulk drug intermediates

Price:
100000 INR
India, Baddi
+91( 
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Description

In- and Out-Licensing, Scientific liaisoning, Audits (planned and unplanned) of bulk drug manufacturers, Supply chain management, New vendor development, Medical writing/CMC writing and Regulatory affairs.

 

-Development of new facility, QC and QA Systems
-Assisting fillings of Drug Master Files in various countries
-Assisting registering products in various countries
-Supporting RA, for timely completion of DMF’s
-Assisting 'How to face Regulatory Audits'
-Assisting to file Dosage forms in various countries
-Assisting Stock and Sale of API's, Finished Dosage forms
-Assurance of all mfg Licenses, GMP, WHO-GMP
-Assist to obtain Indian Drug License, GMP, WHOGMP
-Assisting to get Halal Certificate from Muslim Food Board, Kosher Certificate, and AIB Certificate from American Institute of Bakeries
-Implement internal as well as external Audit system at regular interval with recommendations for a consistent improvement
-Organize trainings for Prodn, QC, QA, and Warehouse
-Perform periodic Internal Audits to ensure that the current systems are in practice
-Perform Vendor Audits for Raw Materials as third party audit, evaluate and recommendation
-Assist effective use of used solvents
-Assist to prepare Tech Packs for various customers
-Assist to prepare of Site Master files
-Prepare,revise SOP's and Standard Testing Procedures for QC, QA Production, Maintenance, Warehouse, HR
-Equipment Qualification and validation
-Process and cleaning validation
-Ensure Plant, Personnel & Equipment Hygiene and Pest Control
-Assist completion of responses for Customer’s Queries, Quality Complaints, and Sample Requests
-Support to Mfg, Warehouse, QC, QA, HR, SHE team for the preparation of Audits
-Support Regulatory Affairs team for Queries updates, responses, fillings of DMF’s
-Assist monitoring of Pest Control in Factory Premises
-Assist effective use of Reference standards, working standards and impurities
-Assist to make Annual Product Quality Reviews
-Prepare and revise Specifications of Raw materials, Intermediates, Finished Products
-Assist for effective use of Reprocessing and Reworking
-Assist implementation of SAP

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Audits, Indenting, Trading of natural products, bulk drug intermediates
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