Research & Development

Research & Development

Research & Development

What are the Different Formats of Pharmaceutical Audits?

What are the Advantages and Disadvantages of Pharmaceutical Quality Audits?

What Are the Types of Quality Audits in the Pharmaceutical Industry?

What Are the Different Types of Audits in the Pharmaceutical Industry?

Case study of Sun Pharma / Caraco (US): Recalls due to contamination and CGMP non-compliance.

Case study of Sandoz Canada (2012): Supply shortages due to non-compliance with GMP.

case study of Ranbaxy Laboratories (India): Data falsification and GMP violations → $500 million settlement with USFDA.

case study of HeLa Cells & Informed Consent: Use of Henrietta Lacks’ cells without permission sparked bioethics debates

case study of Tuskegee Syphilis Study (USA, 1932–1972): Unethical human experimentation leading to stronger clinical research ethics rules.

Case study of Ranbaxy & Glass Particles Recall (2014): Glass particle contamination in injectables.

Case study of Tylenol Cyanide Crisis (1982): Tampering case → led to tamper-proof packaging regulations.

case study of the Heparin Contamination (2008): Over sulfated chondroitin sulfate contamination caused deaths

Case Study: Valsartan Recall (2018): NDMA contamination due to changes in manufacturing process in China.

Case Study – Zolgensma (Novartis): World’s most expensive drug → debates on affordability of gene therapy

Case Study – Gilead’s Remdesivir (COVID-19): Emergency use authorization, pricing and access debates.

Case Study: Pharmacovigilance Signal Detection – Vioxx (Rofecoxib)

Case Study: Supply Chain Disruption – API Shortage

Case Study: Cross-Contamination in a Multi-Product Pharmaceutical Facility

Case Study: COVID-19 Vaccine Development – Pfizer/BioNTech

Case Study: OOS Investigation – Tablet Dissolution

Case Study: Data Integrity Failures – FDA Warning Letters

Advanced Technology transfer Interview questions guide for Injectable Plants (Part 2)

Interview Questions for MSAT / Tech transfer department in Pharma

“Essential Interview Questions on Flow Properties of Powders for Freshers”

“Top Formulation R&D (Oral Solid Dosage) Interview Questions for Experienced Professionals”

“Top 20 Interview Questions on Semi-Solid Dosage Forms for Pharma Freshers”

“Essential Interview Questions on Pellets in the Pharmaceutical Industry”

Methods of Sterilization in the Pharmaceutical Industry

What are Forced Degradation Studies in Pharmaceuticals

Drug-Excipient Compatibility Study

What is Lyophilization?

“Understanding the Distinction Between Oral Tablets and Injectable Medications”

“Understanding the Role of Process R&D in Pharmaceutical Manufacturing”

“Technology Transfer: A Key Pillar in Pharmaceutical Manufacturing”

“The HLB System in Pharma: Importance, Values, and Applications”

“Understanding the Various Routes of Drug Administration: A Complete Guide”

What are Pre-Formulation Studies in Formulation Development

Importance of Binders in Granulation for Pharmaceutical Manufacturing

Myths About Generic Drugs and the Reality

“The Importance of Blending and Blend Uniformity in Pharmaceutical Manufacturing”

Classification of Residual Solvents

What is the difference between Tablets and Capsules

Understanding Dissolution vs. Disintegration in Pharmaceuticals

Calculation Of Bulk Density and Its Importance in Pharma

What is Relative Humidity and significance in Pharmaceutical Industry

What is the difference between moisture content and Loss on Drying

Phyto Somes Overview – A novel drug delivery Approach

Niosomes – A novel drug delivery approach

What is BCS classification for Drugs

Key Excipients in Pellet Formulation – Overview

“Exploring Pharmaceutical Pellets: Techniques involved in Pellets Formulation

Exploring the Film Coating Process in Pharmaceutical Manufacturing

Understanding the Sugar-Coating Process

What is the difference between Absolute Bioavailability and Relative Bioavailability

Disintegration time of Tablets and its Importance

Sublingual tablets and its Types

What is the importance of diluents in tablet Compression

Pharmaceutical Sweeteners

Formulation Development Interview Questions

“Disintegrants and Their Role in Tablet Formulation”

Requirements and Implementation of Continuous Training in Pharmaceuticals

Role of Research and development in Pharmaceutical industry?

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