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Thu. Mar 30th, 2023

Drug master file DMF

Oct 22, 2011

What is drug master file? Drug master file (DMF) is set of documents submitted to food and drugs administration (FDA)…

@timesofpharma Ebola vaccines in development but not fully tested for safety/effectiveness. Vaccine trials ongoing in Liberia & Sierra Leone
— CDC (@CDCgov) November 2, 2015

.@timesofpharma Part 1/2: Some antimicrobial surfaces may help reduce germs in healthcare & require more research #AdiosSuperBacterias
— CDC (@CDCgov) August 6, 2015

.@timesofpharma Part 2/2: These surfaces don’t replace strict infection control, hand hygiene & cleaning/disinfection #AdiosSuperBacterias
— CDC (@CDCgov) August 6, 2015

.@timesofpharma Quitting smoking is best way to slow progression for smokers.
— CDCChronic (@CDCChronic) November 19, 2014

.@timesofpharma People with symptoms should ask MD about breathing test aka spirometry.
— CDCChronic (@CDCChronic) November 19, 2014

.@timesofpharma Quitting smoking is best way to slow progression for smokers.
— CDCChronic (@CDCChronic) November 19, 2014

REMINDER: Join @CHPA 's #OTC Academy on Product Stability: Microbiological Testing, May 17-18 https://t.co/JP12zIP9ZY cc @timesofpharma
— U.S. Pharmacopeia (@USPharmacopeia) May 16, 2016

Clean Room Clean room Classification Pharmaceutical Manufacturing Validation

Restricted access barrier system

Mar 23, 2023

Restricted access barrier system RABS technology for sterile dosage form manufacturing and filling. Sterile dosage form is required to maintain its sterility and it directly...

Pharmaceutical Manufacturing US FDA Guidelines USFDA Inspection

What is 483 observation of USFDA

Mar 18, 2023

What is 483 USFDA observations? Detail information issued by the US FDAs 483 observation form. US FDA is world one of best pharmaceutical regulatory agency,...

Healthcare Information

How to Investigate Out of Speciation results

Mar 15, 2023

What is OOS in pharma, how to Investigate Out of Speciation results. OOS is an abbreviation of term “out of specification” the specification means the...

Pharmaceutical Manufacturing

Compressed air gas for pharmaceutical use

Mar 14, 2023

Compressed air gas for pharmaceutical manufacturing it's limit for microbial count. for sterile product the Total Viable Bacterial count should be lesser or equal to...

Cleaning Validation Hold Time Study

Hold time study in pharmaceutical manufacturing

Mar 13, 2023

Hold time study in pharmaceutical manufacturing. What is hold time study? Good manufacturing guidelines for pharmaceutical manufacturing mentions that a pharmaceutical manufacturing unit must follow...

Pharma Times Latest

Clean Room Clean room Classification Pharmaceutical Manufacturing Validation

Drug master file DMF

Restricted access barrier system

What is 483 observation of USFDA

How to Investigate Out of Speciation results

Compressed air gas for pharmaceutical use

Hold time study in pharmaceutical manufacturing

Pharma Times Latest

Restricted access barrier system

What is 483 observation of USFDA

How to Investigate Out of Speciation results

Compressed air gas for pharmaceutical use

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