OUR TEAM INCLUDES:

  • Project Managers
  • Engineers (Civil, Electrical, Mechanical, Automation, Computer)
  • Architects
  • HVAC Engineer
  • Designers
  • CAD & CAM Specialists
  • Scientists (Laboratory, Pharmaceutical, Regulatory, Formulation,)
  • Pharmacists
  • Chemists
  • Auditors

With our team, we take pride in providing result-oriented, profitable, quality, services.

 

 

 

 

 

aidan

Aidan Madden

Aidan Madden is an experienced IRCA certified Lead Auditor and Qualified person. He has extensive knowledge of Validation, EU GMP Volume 4 Parts 1 & 2, OECD GLP, GDP, ISO 9001:2008, ICHQ7A, ISO 13485. In pharmaceutical Industry he has worked as Quality Control Laboratory Manager in Fort Dodge Labs, Quality Manager in Wyeth Medica, Senior Microbiologist in Baxter. Read more...

 

ann

Ann Mc Garry

Ann has 20 years work experience in manufacturing sector as a Technical Manager with emphasis in Engineering, Healthcare & Pharmaceutical sectors. Her expertise includes Quality Systems, Problem Solving, Process Improvement and Team Building. In addition to her technical qualifications Ann also has extended her portfolio to Training and Coaching helping businesses to release their potential through staff development thereby creating value. Read more... 

 

colin

Colin Booth

Colin Booth started his career as QA Pharmaceutical Microbiology Manager for Astra Zeneca. He leaded 30 staff providing microbiology support to the factory, including management of the QC function. Between 1988-2003 he was Director of Pharmaceutical Microbiology for GSK. Read more...

 

cristina

Cristina Falcão

Cristina Falcão is a Portuguese Lawyer and Pharmaceutical Consultant as well as a consultant on cold chain and supply chain (supporter of technology innovation relating to pharmacies and supply chains; assistant to a major supplier of pharmacy logistics databases, testing and assuring quality). Read more...

 

destin

Destin A. LeBlanc

Destin A. LeBlanc is an internationally recognized expert in the area of cleaning and cleaning validation for pharmaceutical process equipment. Mr. LeBlanc has thirty years of product development and technical service experience, primarily in cleaning and antimicrobial applications. Read more...

 

dominic

Dominic Parry

Dominic has worked in the pharmaceutical industry since 1992, and is a leading pharmaceutical quality management specialist.  He worked for 4 years at Evans Medical Limited (now Novartis Vaccines) as a Production Development Scientist.  He then moved to Hoechst Marion Roussel (now Patheon, UK), where he worked for 4 years as a Quality Assurance Officer and then Validation Manager for the sterile manufacturing operations. Read more...

 

doug

Douglas Thorogood Ph.D

Douglas Thorogood Ph.D is an experienced international consultant in areas of facility design, sterility assurance, regulatory affairs and containment technology. He successfully implemented new facility design and qualification for three Baxter Travenol facilities  in UK and USA . He was responsible for preparation of document trail for registration and regulatory. He has successfully implemented isolator technology in large pharmaceutical groups replacing clean rooms with various designs of isolators for containment during compounding of toxic materials and aseptic filling of cytotoxics, vaccines and heat labile pharmaceutical preparations. Read more... 

 

emil

Emil Walter Ciurczak Ph.D

Emil W. Ciurczak has degrees in Analytical and Physical Chemistry from Rutgers and Seton Hall Universities. He has worked in pharmaceutical companies, performing analytical method development and method improvements, designing and modifying analytical devices. He is the winner of the EAS (2004) Award for Contributions to NIR. Read more...

 

graeme

Graeme Ladds

Dr. Graeme Ladds has been involved in Drug Safety for the last 20 years and his last role in industry was Head of Global Drug Safety at Shire Pharmaceuticals. Nine years ago, Graeme set up his own consulting Company PharSafer Associates Ltd, a niche CRO providing both Clinical and post marketing drug safety and medical information services to the Pharma industry globally, from total outsourcing of Safety and Medical Services to bespoke projects and interim requirements. Read more...

 

hedley

Hedley Rees

Hedley Rees is a practising consultant, coach and trainer, helping healthcare companies build, manage and continuously improve their clinical trial and commercial supply chains and risk profiles. Prior to this, Hedley held senior supply chain positions at Bayer, British Biotech, Vernalis, Johnson & Johnson and OSI Pharmaceuticals. Read more...

 

michael

Michael J. Miller Ph.D

Michael J. Miller Ph.D is an internationally recognized microbiologist and subject matter expert in pharmaceutical microbiology and the design, validation and implementation of rapid microbiological methods. In this role, he is responsible for providing scientific, quality, regulatory and business solutions for the pharmaceutical industry and suppliers of new microbiology technologies. Read more...

 

peter

Peter John Lavis

Peter is a Quality Management Systems specialist, with extensive experience from outside and inside the pharmaceutical industry.  This allows him to effectively "critique and challenge" how things are done in the pharmaceutical industry. Read more...

 

robert

Robert Haslam

Robert Haslam is a practising EU Qualified Person and Qualified Pharmaceutical Lead Auditor. He is a pharmaceutical industry VP with over 35 years of experience in Quality Assurance, Production, Development, Clinical Trials, Regulatory Affairs gained in multinational and start-up companies. ISO-Qualified Lead Auditor with extensive experience in GMP audits of drug substance, drug product and investigational Medicinal Product manufacturers worldwide to meet FDA and EU requirements. Read more...

 

saeed

Saeed Qureshi, Ph.D.

At present, Dr. Qureshi’s focus is in providing training and/or consultation in the area of drug dissolution testing. Specifically covering topics such as fundamentals of the testing, method development/validation, product development/evaluation, establishing in vitro-in vivo corrections (IVIVC) and bio-waivers, troubleshooting (standardization and calibration), and cost savings. Read more...

 

tim

Tim Sandle Ph.D

Dr. Sandle is the Head of Microbiology at Bio Products Laboratory Limited (a pharmaceutical organization owned by the UK Department of Heath).  Dr. Sandle is a chartered biologist (Society for Biology) and holds a first class honours degree in Applied Biology; a Masters degree in education; and obtained his doctorate from Keele University. Read more... 

 

 

tim

Sait Uluözyurt

Sait graduated from Gazi University, Department of Chemical Engineering as Chemical Engineer.. He has worked in several different local and multi national pharmaceutical and API Manufacturing facilities during his more than 30 years of experience. Read more... 

 

tim

Alp Kırmaz

Alp Kırmaz is graduated from Chemical Engineering department of Boğaziçi University in 1994 and has completed his master study in the same department in 1997. He has started his career in Eczacıbaşı Pharmaceuticals as Galenical Development Engineer. After working two years in this position Read more... 

 

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