Gmp Certification - Pharma

Relevant Publications

Regulatory Frameworks for Advanced Therapy Medicinal Products in Thailand.

Issue Release: 2023

Acute Toxicity and Pharmacokinetic Profile of an EU-GMP-Certified L. in Rodents.

Issue Release: 2023

Regenerative Potential of Stem Cell-derived Extracellular Vesicles in Spinal Cord Injury (SCI).

Issue Release: 2022

Compliance in Non-Clinical Development of Cell-, Gene-, and Tissue-Based Medicines: Good Practice for Better Therapies.

Issue Release: 2022

[Management system and development strategy of quality Chinese medicine].

Issue Release: 2021

New Challenges for Biobanks: Accreditation to the New ISO 20387:2018 Standard Specific for Biobanks.

Issue Release: 2021

Assessing the Performance of Food Safety Management System Using Food Safety Management System Diagnostic Tools and Microbial Assessment Scheme: A Case of Powdered Beverage Manufacturers.

Issue Release: 2021

MSC Manufacturing for Academic Clinical Trials: From a Clinical-Grade to a Full GMP-Compliant Process.

Issue Release: 2021

Cost benefit of investment on quality in pharmaceutical manufacturing: WHO GMP pre- and post-certification of a Nigerian pharmaceutical manufacturer.

Issue Release: 2017

Good Manufacturing Practice-Compliant Production and Lot-Release of Expanded Regulatory T Cells As Basis for Treatment of Patients with Autoimmune and Inflammatory Disorders.

Issue Release: 2017

Comparison of food colour regulations in the EU and the US: a review of current provisions.

Issue Release: 2017

[Analysis of several key problems of good agricultural practice (GAP) of Chinese materia medica].

Issue Release: 2016

[Preliminary study on suitability of ozone sterilization in traditional Chinese medicine and its preparation].

Issue Release: 2015

Deterministic and stochastic approaches in the clinical application of mesenchymal stromal cells (MSCs).

Issue Release: 2014

Role of the blood service in cellular therapy.

Issue Release: 2011

Developments in consultancy and training in the GLP arena: 1980 to 2020. A personal view.

Issue Release: 2008

WHO Expert Committee on Specifications for Pharmaceutical Preparations.

Issue Release: 2003

Remune. Immune Response.

Issue Release: 2002

The need for good practices in biomedical technology.

Issue Release: 1996

Similarities and Differences of International Practices and Procedures for the Regulation for Active Substance Master Files/Drug Master Files of Human Use: Moving Toward Regulatory Convergence.

Issue Release: 0000

What is Geriatric Care in Pharma?

What Are the Challenges of Clinical Trials?

What is Cellular Stress?

How Are Participants Protected?

Why is Transitional Care Important in Pharma?

What Should Be Included in Patient Education Materials?

What Role Does Regulatory Affairs Play?

Why is Patient Education Important?

What is Pharma?

What Challenges Do Pharmacists Face?

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