A day in the life of an RP
Natwest Accelerator Masterclass Natwest Accelerator Master class As an independent Pharmaceutical Responsible Person Consultant, running my own business, I specialize in helping SME Pharmaceutical Wholesalers implement robust Quality Management Systems. One of the greatest perks of entrepreneurship is the chance to attend inspiring business events. Recently, I had the privilege of participating in the Natwest […]
Current Vacancy
Quality Specialist/Trainer Required The Importance of QA Specialist We are thrilled to announce the development of accredited training programs specifically focused on Responsible Person (RP) coaching and Responsible Person Import (RPi) training, integration of AI and the Pharmaceutical Quality Management system. This is why we are seeking a dedicated QA Specialist Trainer in the pharmaceutical […]
Application of Critical Analysis in Deviation Management- 9 reasons why
Application of Critical Analysis in Deviation Management- 9 reasons why Introduction The Medicines & Healthcare Products Regulatory Agency (GMDP Symposium 2016) stated the common deficiencies found in deviation management systems and CAPAs as listed below: Deviations were not adequately documented and investigated, consequently the appropriate CAPAs were not implemented. The investigations lacked the […]
Data Integrity Work Shop
I attended a work shop on Data Integrity; this is a very challenging area for majority of pharma companies, these challenges vary from company to company. This is also a major area of focus for the regulatory bodies. Embedding data integrity in pharmaceutical QMS not only instils complete confidence in pharmaceutical products by the end […]
MHRA GMDP Symposium
I will be at the MHRA GMDP Symposium event 06 & 09 December. An opportunity to share concerns and learn directly from the MHRA. The GMDP event is ideal for pharmaceutical industry professionals in quality control and quality assurance, regulatory and compliance involved in manufacturing medicines and is complemented by the GDP event which covers […]
Data Integrity: Asset or Liability
Data Integrity: Asset or Liability Introduction Data integrity (DI) is fundamental in any pharmaceutical quality system; this ensures that medicines are of the required quality, safety and efficacy. Data integrity refers to the overall completeness, accuracy and consistency of data during its entire life cycle. The data lifecycle considers the entire phases in the […]
The Importance of Data Integrity in Pharmaceutical Quality Management System
The Importance of Data Integrity in Pharmaceutical Quality Management System The MHRA (2015) states “Data integrity (DI) is fundamental in a pharmaceutical quality management system which ensures that medicines are of the required quality and the data governance system should be integral to the pharmaceutical quality system described in EU GMP chapter 1.” Furthermore […]