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Tag: Lovlina Borgohain Medal

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Lovlina Borgohain :2nd Medal Hope for India

Sushmita4 years ago3 years ago06 mins

After defeating China’s Nien-Chin Chen in women’s welter Lovlina Borgohain has won the quarter-finals under the 64-69 kg category, she now assures a second medal at the 2020 Tokyo Olympics. She won the last match with an easy win of a split of 4-1 and is ready for the semi-finals against turkey’s Busenaz Burmeneli will…

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Pharmaceuticals

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What effect does X-ray inspection have on pharma products?

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How counterfeiters are breaching India’s QR code system

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Lyophilization: Principles, Process, and Applications

4 years ago3 years ago
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  • Pharmaceuticals & Biologics

Drug Design: Matching a Drug to Its Target

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Pharma 4.0: The Future of Pharmaceutical Manufacturing

4 years ago3 years ago
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Understanding ANDA Submission Requirements: A Key to Affordable Medicine

4 years ago3 years ago
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Pharmaceutical QA: Understanding and Implementing ICH Q9 Guidelines

4 years ago3 years ago
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  • Pharmaceuticals & Biologics

Understanding FDA’s Deficiency Response Letters for ANDA Submissions: A Guide to Successful Outcomes

4 years ago3 years ago
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  • Pharmaceuticals & Biologics

Mastering Post-Approval Changes in Pharma: Key Strategies for Compliance and Efficiency

4 years ago3 years ago
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Understanding Process Analytical Technology (PAT) Tools: Revolutionizing Pharmaceutical Manufacturing

4 years ago3 years ago
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  • Pharmaceuticals & Biologics

Do you review or Do you preview ?

4 years ago3 years ago
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  • Pharmaceuticals & Biologics

Process Validation in the Pharmaceutical Industry: Ensuring Consistency and Quality

4 years ago3 years ago
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  • Pharmaceuticals & Biologics

What is CAPA and Why It’s Mandatory in Pharmaceuticals?

4 years ago3 years ago
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Understanding Critical Quality Attributes (CQA) and Critical Process Parameters (CPP) in Pharmaceuticals

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Ensuring Compliance with 21 CFR Part 11 in Pharmaceuticals

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GLP-1 Single, Dual, and Triple Receptor Agonists for Treating Type 2 Diabetes and Obesity: A Comprehensive Narrative Review

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What is Data Integrity and Its Importance in Pharmaceuticals?

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Everything You Need to Know About LC-MS Sample Preparation

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What is HPLC, Why is it Important in Pharma, and What are its Phases?

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  • Pharmaceuticals & Biologics

 Challenges and Complications of Poly(lactic coglycolic acid)Based Long Acting Drug Product Development

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Extrapolation and Regression Study

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 Applications of Polymers in Parenteral Drug Delivery

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  • Pharmaceuticals & Biologics

What is GxP Training and Why is It Important?

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Validation of Sterile Filtration: A Comprehensive Overview

4 years ago3 years ago
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Digital Transformation in the Pharmaceutical Industry: How web-based applications and softwares are paving the way for AI integration

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Unlocking the Power of LCMS: A Comprehensive Guide to Liquid Chromatography-Mass Spectrometry

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What Are Pharmaceutical Quality Control Laboratories and Why Are They Important?

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  • Pharmaceuticals & Biologics

 Phospholipids in Depot Formulations: A Comprehensive Overview

4 years ago3 years ago
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What Are Stability Guidelines and Their Importance in the Pharmaceutical Industry?

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  • Pharmaceuticals & Biologics

 In Vitro–In Vivo Correlation on Parenteral Dosage Forms: A Detailed Analysis

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What is GMP Environmental Monitoring Management and How it Helps the Pharmaceutical Industry?

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How to Improve Your Ability to Read Nutrition Research?

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Drug-Device Combination Products: Methodologies for User Interface Evaluation

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Quality Control vs Quality Assurance vs Total Quality Management: Understanding Their Role and Importance in the Pharmaceutical Industry

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In Vitro Release Test (IVRT) for In Situ Gel/Depot-Forming Drug Products

4 years ago3 years ago
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  • Pharmaceuticals & Biologics

Detailed Explanation of Teriparatide Generic Approval Process

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ALCOA vs. ALCOA++: Understanding Data Integrity in the Pharmaceutical Industry

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Explore 5 lucrative intellectual property career paths for science graduates. Discover how to leverage your scientific expertise in patent law, technology transfer, and IP management.

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  • Pharmaceuticals & Biologics

Why Risk Assessment and Mitigation Controls Reporting is Mandatory for QA and How to Handle It

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Cluster Development Programme (CDP) & Data Governance: Why It’s Mandatory and How to Handle It in the Pharmaceutical Industry

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Extractables and leachables: definitions, differences & facts

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Visible Particles in Parenteral Drug Products: A Review of Current Safety Assessment Practice

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The Role of Statistics in Clinical Trials: Safeguarding Patient Safety and Improving Healthcare Outcomes through Rigorous Evaluation of Medical Treat.

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Why DQ, IQ, OQ, PQ Are Mandatory in Quality Assurance: Why It’s Essential and How to Handle It

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Cleaning Validation and Verification Reporting: A Mandatory QA Requirement

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Handling Elemental Impurities Risk Assessments in Pharmaceuticals

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Leading Hidradenitis Suppurativa Treatments in the Market

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Exploring Pharmacokinetic (PK) Data and Strategies for Analysis

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Bristol Myers Squibb Advances Opdualag to Phase 3 Trials for Non-Small Cell Lung Cancer

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Keytruda’s Triumph in Early-Stage Triple-Negative Breast Cancer: A New Standard of Care

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GSK Advances mRNA Flu Vaccine to Late-Stage Trials Following Positive Mid-Stage Results

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AI and Biosimilars: Bridging Global Health Disparities and Enhancing Treatment Efficiency

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The Importance of Chemistry, Manufacturing, and Controls (CMC) Regulatory Documentation in Pharmaceuticals

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Drug scheduling

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The Crucial Role of Preformulation Studies in Drug Development

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What Are Some Types of Long-Acting Injectables?

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Extractables and Leachables

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Persist AI and Nivagen to Collaborate on AI-Driven Manufacturing Process for Long-Acting Injectable

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