drugregulatoryaffairs.wordpress.com
M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/2012/02/02/m3r2-qas-on-combination-drug-toxicity-testing-available-on-the-ich-website
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
FDA issues guidance on Advertising and Promotional Labelling « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/2012/01/31/fda-issues-guidance-on-advertising-and-promotional-labelling
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
ICMR « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/icmr
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
FDA: Forms 0356h and 2252 has updated « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/2012/01/17/fda-forms-0356h-and-2252-has-updated
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
CDSCO plans to set up 20 mini labs at sea ports, airports « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/2012/02/06/cdsco-plans-to-set-up-20-mini-labs-at-sea-ports-airports
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
Government pushing for tough new law to regulate drug trials « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/2012/01/09/government-pushing-for-tough-new-law-to-regulate-drug-trials
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
Policy & Regulations + Font Resize – CDSCO plans permanent ‘India country office’ for pharmaceuticals in 5 overseas locations « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/2012/01/09/policy-regulations-font-resize-cdsco-plans-permanent-india-country-office-for-pharmaceuticals-in-5-overseas-locations
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
CDSCO « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/cdsco
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
SFDA Announcement – Implementation of eSubmission for human pharmaceuticals « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/2012/01/17/sfda-announcement-implementation-of-esubmission-for-human-pharmaceuticals
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
drugregulatoryaffairs.wordpress.com
EMA: EU Module 1 eCTD Specification v1.4.1 – Published « DRUG REGULATORY AFFAIRS
https://drugregulatoryaffairs.wordpress.com/2012/01/17/ema-eu-module-1-ectd-specification-v1-4-1-published
Just another WordPress.com site. WHO Publishes Draft on Process Validation. CDSCO plans to set up 20 mini labs at sea ports, airports. M3(R2) Q&As on Combination Drug Toxicity Testing available on the ICH website. CRO’s and Clinical Research in India. FDA issues guidance on Advertising and Promotional Labelling. EMA: EU Module 1 eCTD Specification v1.4.1 Published. FDA: Forms 0356h and 2252 has updated. SFDA Announcement Implementation of eSubmission for human pharmaceuticals. Regulatory News / Updates.
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