Pharma Digests

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Viewing 15 posts - 1 through 15 (of 15 total)

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March 9, 2025 at 8:55 am in reply to: EU GMP Audit #6861
FRD
Participant
Are EU and FDA GMP audits similar?
March 9, 2025 at 8:49 am in reply to: FDA GMP Inspection #6860
FRD
Participant
What areas of a pharmaceutical industry fall under the scope of FDA GMP inspections?
December 11, 2024 at 1:42 am in reply to: Drug Layer Coating #6580
FRD
Participant
You should optimize the spray rate, inlet air temperature and atomization air pressure.

High spray rate and high inlet temperature need to skip!
September 15, 2024 at 1:24 am in reply to: Pharmaceutical Finished Product Analysis #6265
FRD
Participant
Is it mandatory to follow the monograph test method always?
September 15, 2024 at 1:22 am in reply to: Biowaiver #6264
FRD
Participant
What are the risk factors for getting BCS based biowaiver?
September 15, 2024 at 1:13 am in reply to: EU GMP Audit #6263
FRD
Participant
Is it sufficient to get approval from any EU members for whole EU market?
September 15, 2024 at 1:09 am in reply to: Most Stringent Regulatory Authorities #6262
FRD
Participant
What is the difference between most stringent and less stringent regulatory authority?
September 15, 2024 at 1:07 am in reply to: Imprinting of Solid Oral Dosage Form #6261
FRD
Participant
If the product is more sticky in nature, how to debossed on it?
September 15, 2024 at 12:59 am in reply to: Lyophilized Product Development #6258
FRD
Participant
Why only liquid nitrogen is used in lyophilization process?
August 31, 2024 at 9:48 am in reply to: Clinical Pharmacy Specialist #6232
FRD
Participant
What are the major role of clinical pharmacist?
August 8, 2024 at 5:26 am in reply to: QMS Tools #6108
FRD
Participant
What are the six pharmaceutical quality systems as defined by FDA?
July 25, 2024 at 5:34 am in reply to: FBP Process Scale-Up #6093
FRD
Participant
Which parameters can keep same/similar during FBP process scale-up?
July 18, 2024 at 8:41 am in reply to: Imprinting of Solid Oral Dosage Form #6092
FRD
Participant
Is it mandatory for oral solid dosage drug product to use imprint code?
June 24, 2024 at 4:12 am in reply to: Bioequivalence Study of Generic Drugs #6040
FRD
Participant
Which physicochemical properties of API should be considered for Bio study?
May 9, 2024 at 6:31 am in reply to: Valsartan + Amlodipine Tablets #5965
FRD
Participant
Is there any challenge on analytical method of Valsartan + Amlodipine Tablets?
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Viewing 15 posts - 1 through 15 (of 15 total)