PharmaTech

OCTOBER 15, 2024

Discover how end-to- end integrated automation systems can streamline your processes, improve flexibility, reduce time-to-market, maximize revenue, and drive continuous improvement. Transform your pharmaceutical manufacturing processes today!

Process Improvement 52

Process Improvement Pharmaceutical Manufacturing 52

GMPSOP

JANUARY 29, 2025

Fundamental requirements of GMP compliant software The critical objectives for developing a quality management software application are to make the quality concern investigations processes faster, more reliable, accurate, secure, and permanent for future reference.

Documentation 94

Documentation Process Improvement Pharmaceutical Manufacturing 94

Express Pharma

MARCH 12, 2025

It attributed Indias cost advantage to high-production capacity plants, process improvements, economies of scale, and backward integration in manufacturing. IPA also addressed concerns regarding transparency in drug manufacturing locations.

Generic Medicine 66

Generic Medicine Process Improvement Dosage Pharmaceutical Manufacturing 66

GMPSOP

MARCH 17, 2023

For instance, you can undertake a list of process improvement works targeting the elimination of causes that have resulted in the defect. A robust CAPA process is an ongoing effort, with a focus on continuous improvement, and is a key requirement for compliance with regulatory bodies.

Documentation 52

Documentation Packaging Process Improvement Pharmaceutical Manufacturing 52

Drug Patent Watch

JANUARY 9, 2025

Managing Quality and Compliance Quality and regulatory compliance are non-negotiable in pharmaceutical manufacturing. Ensuring Data Integrity Data integrity is paramount in pharmaceutical manufacturing. Ensure your CDMO has robust systems in place to maintain data integrity throughout the manufacturing process.

Communication 52

Communication Drug Development Pharmaceutical Manufacturing Process Improvement 52