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cGMP

April 14, 2018
Pharmaceutical Articles

Validation, Qualification and Calibration: The 3 Most Crucial Processes of a Pharma Industry

A lot of transformations in the pharmaceutical industry over a period of time have fueled an increase in the outsourcing of activities such as validation, qualification, calibration, auditing etc. Transformations such as the boost in R&D expenses, expiring patents of path-breaking medicines, resulting in

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February 4, 2016

Effects of Pharmaceutical CGMPs on Innovation in the Pharmaceutical Industry

There are numerous innovations that have been made in the pharmaceutical industry.

April 22, 2015

Equipment Qualification Process: Calibration and Validation

[wp_ad_camp_4]In the pharmaceutical word, it’s extremely important to qualify and validate equipment

Telstar at CPhI Milan 2021
Pharmaceutical Articles

Telstar promotes 360º solutions at CPhI Worldwide-2021

October 29, 2021

Terrassa (Barcelona). Telstar will be actively participating at CPhI, to be held in Milan, during 9-11th November 2021, promoting its personalized

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Pharmaceutical Articles

Validation, Qualification and Calibration: The 3 Most Crucial Processes of a Pharma Industry

April 14, 2018

A lot of transformations in the pharmaceutical industry over a period of time have fueled an increase in the outsourcing

More
Pharmaceutical News

Quotient Clinical incorporates Japanese bridging into a Translational Pharmaceutics® program

March 15, 2016

Quotient Clinical, the Translational Pharmaceutics company, has announced the completion of its first clinical program involving Japanese healthy volunteers. The

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Pharmaceutical Articles

Effects of Pharmaceutical CGMPs on Innovation in the Pharmaceutical Industry

February 4, 2016

There are numerous innovations that have been made in the pharmaceutical industry. Scientists/ researchers are spending endless nights coming up

More
Pharmaceutical Articles

Equipment Qualification Process: Calibration and Validation

April 22, 2015

[wp_ad_camp_4]In the pharmaceutical word, it’s extremely important to qualify and validate equipment and procedures, in order to not only adhere

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