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FOPE, PharmaState Academy, complete one year of the PULSE program

Express Pharma

He noted frequent gaps in team understanding due to staff turnover and stressed the need for strong communication, confidentiality, and documentation practices. Emphasis was placed on treating contracts as living documents and aligning all operational actions with documented expectations.

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Session 21 of FOPE, PharmaState Academy’s PULSE Program, advances excellence in manufacture of APIs under revised schedule M

Express Pharma

The session concluded with a strong push for systematic documentation and continuous compliance vigilance in line with global GMP. He explained that stability testing must simulate market packaging to justify shelf life or retest dates. For inquiries or to pre-book participation, visit PharmaState Academy’s official website.

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FDA Issues “Cliffs Notes”-style Guidance on Cell and Gene Therapy; What Questions Did They Answer? (Part 1)

FDA Law Blog: Biosimilars

As much of the content of this draft guidance for cellular and gene therapy (CGT) products is articulated elsewhere, this document serves as a one-stop shop or Cliffs Notes for the numerous guidance documents now covering CGT product development. CBER will not commit to reviewing packages greater than 250 pages.

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Financial Due Diligence in the Med Spa Industry: Key Considerations

Beckers Hospital Review

This volatility stems from the use of prepaid and packaged services, membership offerings, and gift card sales, each necessitating adjustments to accurately reflect revenue generation within a given period. This process ensures accurate revenue recognition under ASC 606 as we transition from cash to accrual accounting.

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Episode 864: Why Did ISMP Remove the Do Not Crush List from Their Website?

Pharmacy Joe

Subscribe on iTunes , Android , or Stitcher If you navigate to the page on the website for the Institute for Safe Medication Practices that once hosted the document titled “Oral Dosage Forms That Should Not Be Crushed” you will instead find a notice that the list has been removed from the ISMP website.

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Pharmaceutical sampling procedures for non-sterile products

GMPSOP

Starting materials are processed, sampled, tested, packaged, and released before the finished products are stacked on pharmacy shelves. Sampling is carried out on intermediate processed materials and tested to ensure those are formulated correctly, free from contamination and qualified for filling and packaging. as their visual aids.

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How to conduct GMP training for employee

GMPSOP

GMP/GLP and PPE training are applied to all employees, contractors and casual staff working in a GMP environment, including manufacturing, packaging, labelling, distribution, QA, QC, development, validation, engineering, IT staff and anyone whose activities could affect product quality. Additional documents are included each month.