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Raaj Global Pharma RA Consultants | TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION

TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION

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Raaj Global Pharma RA Consultants | TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION | raajgprac.wordpress.com Reviews

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TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION

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Admission OPEN for Regulatory Affairs, CTD/eCTD, QA, CLINICAL, Pharma Documentation, Pharmacovigilance, Patents Laws and Procedures | Raaj Global Pharma RA Consultants

https://raajgprac.wordpress.com/2012/07/30/admission-open-for-regulatory-affairs-ctdectd-qa-clinical-pharma-documentation-pharmacovigilance-patents-laws-and-procedures

Raaj Global Pharma RA Consultants. TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION. CTD and eCTD in API. CTD and eCTD in Formulation. Patents Laws and Procedures. Quality Assurance and Quality Management. Admission OPEN for Regulatory Affairs, CTD/eCTD, QA, CLINICAL, Pharma Documentation, Pharmacovigilance, Patents Laws and Procedures. Admission OPEN for Regulatory Affairs, CTD/eCTD, QA, CLINICAL, Pharma Documentation, Pharmacovigilance, Patents Laws and Procedures. July 30, 2012. Regulatory su...

2

CHMP Guidance on Process Validation | Raaj Global Pharma RA Consultants

https://raajgprac.wordpress.com/2012/08/08/chmp-guidance-on-process-validation

Raaj Global Pharma RA Consultants. TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION. CHMP Guidance on Process Validation. CHMP Guidance on Process Validation. August 8, 2012. Guideline on Process Validation 12. 51 Traditional process validation……………………………………………………………………. 4. 52 Continuous process verification …………………………………………………………………. 5. Guideline on Process Validation EMA/CHMP/CVMP/QWP/70278/2012-Rev1 Page 2/11. Leave a Reply Cancel reply. Enter your comment here. Address never made public).

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TOP TEN DEFICIENCIES New Applications for Certificates of Suitability | Raaj Global Pharma RA Consultants

https://raajgprac.wordpress.com/2012/08/04/top-ten-deficiencies-new-applications-for-certificates-of-suitability

Raaj Global Pharma RA Consultants. TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION. TOP TEN DEFICIENCIES New Applications for Certificates of Suitability. TOP TEN DEFICIENCIES New Applications for Certificates of Suitability. August 4, 2012. Top ten deficiencies found after first assessment of new applications in 2011. TOP 1 (3.2.S.2.3): Absence of discussion on the carry-over of impurities/by-products from key materials in the process:. Pls visit : http:/ www.edqm.eu. August 6, 2012 at 11:04 am.

4

rajashriojha | Raaj Global Pharma RA Consultants

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Raaj Global Pharma RA Consultants. TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION. RECALL AND RAPID ALERT SYSTEM FOR DRUGS. November 11, 2012. Published on the website of www.cdsco.nic.in. The following draft guidelines is hereby published as required for NRA assessment by WHO. Objections or suggestions, if any may be addressed to the, Drugs Controller General (India), Central Drugs Standards Control. Organisation, FDA Bhawan, New Delhi 110002. or email id. dci@nic.in. Before the expiry of.

5

RECALL AND RAPID ALERT SYSTEM FOR DRUGS | Raaj Global Pharma RA Consultants

https://raajgprac.wordpress.com/2012/11/11/recall-and-rapid-alert-system-for-drugs

Raaj Global Pharma RA Consultants. TRUST OUR EXPERIENCE TO MANAGE YOUR REGULATORY SUBMISSION. RECALL AND RAPID ALERT SYSTEM FOR DRUGS. RECALL AND RAPID ALERT SYSTEM FOR DRUGS. November 11, 2012. Published on the website of www.cdsco.nic.in. The following draft guidelines is hereby published as required for NRA assessment by WHO. Objections or suggestions, if any may be addressed to the, Drugs Controller General (India), Central Drugs Standards Control. Before the expiry of. A period of fifteen days.

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