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Bangladesh Pharmacists’ Forum Announces New Executive Committee of Gono Bishwabidyalay Unit
Dhaka, June 14: The Central Parliament of the Bangladesh Pharmacists’ Forum (BPF) has approved the new Executive Committee and Advisory Panel of the Gono...
Rotary Tablet Compression Technology, GMP Compliance & Pharmaceutical Documentation Framework
PHARMA NEWS BD, Special Manufacturing Report.
Dhaka, Bangladesh – In a major step toward strengthening pharmaceutical manufacturing knowledge and compliance awareness, a comprehensive technical and...
Tablet Granules Consistency & Density (Bulk and Tapped)
PharmaNewsBD Feature
Tablet Granules Consistency & Density (Bulk and Tapped): Critical Quality Factors in Pharmaceutical Manufacturing
Dhaka, Bangladesh – February 2026 — In pharmaceutical tablet manufacturing,...
Tablet Manufacturing Workflow and Checklist
PharmaNewsBD: Tablet Processing Checklist, designed to support manufacturers in ensuring consistent quality, regulatory compliance, and operational efficiency across all stages of tablet production.
Process validation...
Rotary Tablet Compression Technology, GMP Compliance & Pharmaceutical Documentation Framework
PHARMA NEWS BD, Special Manufacturing Report.
Dhaka, Bangladesh – In a major step toward strengthening pharmaceutical manufacturing knowledge and compliance awareness, a comprehensive technical and...
Tablet Granules Consistency & Density (Bulk and Tapped)
PharmaNewsBD Feature
Tablet Granules Consistency & Density (Bulk and Tapped): Critical Quality Factors in Pharmaceutical Manufacturing
Dhaka, Bangladesh – February 2026 — In pharmaceutical tablet manufacturing,...
Tablet Manufacturing Workflow and Checklist
PharmaNewsBD: Tablet Processing Checklist, designed to support manufacturers in ensuring consistent quality, regulatory compliance, and operational efficiency across all stages of tablet production.
Process validation...
Tablet Manufacturing Defects & Processing Problems: Key Challenges and Preventive Strategies in Pharmaceutical Production
Dhaka, Bangladesh – February 2026 — Tablet manufacturing remains one of the most widely used dosage forms in the pharmaceutical industry. However, despite technological...
(URS) User Requirement Specification of Equipments
Preparation of user requirement specification of equipments and instrument used in pharmaceutical manufacturing and quality control.
User Requirement Specification (URS) is a list of all...
Pharmaceutical quality control (QC)
Pharmaceutical quality control is a critical aspect of the pharmaceutical industry, ensuring the safety, efficacy, and consistency of medications. It involves a series of...
Tablet Manufacturing Workflow and Checklist
PharmaNewsBD: Tablet Processing Checklist, designed to support manufacturers in ensuring consistent quality, regulatory compliance, and operational efficiency across all stages of tablet production.
Process validation...
Below 121 °C is called Low-Temperature Sterilizatio and Its Validation
sterilization is done for heat sensitive material at lower temperature below 121 °C and its validation using Bacillus subtilis (Bacillus atrophaeus) ) ATCC 5230...
Contamination Control Strategies: A Path for Quality & Safety
Controlling contamination of sterile drug products has been a challenge for the pharmaceutical industry for years. Product contamination and the failure to establish and...
Exclusive Talkshow Pictures
Below 121 °C is called Low-Temperature Sterilizatio and Its Validation
sterilization is done for heat sensitive material at lower temperature below 121 °C and its validation using Bacillus subtilis (Bacillus atrophaeus) ) ATCC 5230...
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