Pharma and Device Consultants

Dr. Chen Lim has in-depth and broad pharmaceutical experience through working with multi-national companies (J & J, Janssen-Cilag Pharmaceutical, ICI Pharmaceutical, Schering Plough). He provides consulting on TGA (Australian), NZ, EU, FDA, SFDA and Asian GMP requirements and regulatory compliance.

Our dynamic world of technology is characterized by incessant change. Which means it’s good to have a constant, an invariable, a dependable partner who will be on standby, ready to help whenever you need him. MGroup Engineering has been that kind of partner for over 35 years.

If you want to meet and match the challenges of tomorrow you have to invest in quality planning. That is what we stand for. We pursue the consistent application and improvement of our integrated QM system with the necessary flexibility and dynamism, creativity and innovative energy in every phase of our facilities and systems.

Whether the projects are in engineering, consulting or management, our energies are constantly directed at fulfilling our customers’ expectations on time and on a solid commercial basis.

Place your trust in us, and we can shape the future together.

Quality Management Documents and Templates by download for the pharmaceutical, device, food, API industry. High quality forms and Quality Manuals.

Yeldell Scientific is a science driven company. They help the Pharma, Biotech, Medical, Manufacturing, Engineering and Technical Writing industry achieve their goals by improving their efficiency and reducing costs and operational deviations during documentation processes so that more time and focus can be spent on the quality of the work involved.

Experienced staff includes MS Office software developers, technical writers, scientists and technical trainers. With experience in pharmaceutical software development and professional science writing staff fluent in document automation, GxP regulations, Non-clinical study requirements, documentation workflows, regulated change controls, study management, technical lab activities and the documentation requirements, gaps, needs and software wishes for all mentioned.

TAKE Solutions offers the PharmaReady™ fully compliant Document & eSubmission Management Suite based on Microsoft Windows technology. PharmaReady is a fully integrated, regulatory compliant, web-based Document Management, Training Records Management, Structured Product Labeling, and eCTD Publishing Solution Suite. PharmaReady makes eSubmissions easy to understand, easy to use, and easy to manage.

Consultants who help FDA / GMP, Mil. Spec. and commecial companies become more effective in electronic and PCB design for manufacturability, manufacturing methods and processes, supplier quality control and failure analysis to root cause correction. We accomplish this by helping identify and focus on key and critical functions of their electronic designs affecting manufacture and quality of their products. We use industry tested tools, methods and techniques to identify cost and risk drivers associated with product designs and manufacturing systems.

PharmOut is a consultancy of 40 professionals working throughout the Asia Pacific Region. PharmOut is a boutique consultancy to the Pharmaceutical, Medical Device and Veterinary industries. We specialise in FDA and TGA GMP compliance, validation and continuous improvement. We offer EDMS product, MASTERControl and a number of Training Options.