PharmEng supports Pharmaceuticals, Biologics, Over-The-Counter (OTC), Animal Health, Radiopharmaceuticals, Clinical Trial Products, Medical Devices, Combination Products, Natural Health Products, Personal Care, Disinfectants, and Active Pharmaceutical Ingredients (API) to achieve the most cost-effective way to undertake their regulatory activities worldwide. This includes regulatory intelligence and strategy, worldwide product registration, preparation of regulatory documents, in country representation, establishment registration, and[…..] […]
Read More…
Our clients understand the importance of establishing a robust quality system; The effort in maintaining a strong quality system not only ensures that the products and services meet the customer expectations and fulfill the regulatory requirements, it directly benefits our clients’ business through effective production process and successful regulatory audits. We have many years of[…..] […]
Read More…
PharmEng Technology has recognized that Project Management is becoming an ever-increasing skill requirement throughout Pharmaceutical, Biotechnology and Medical Device industries. Project Management is undoubtedly a key discipline in any company or institution. Proper project management allows for, among other things: Reduce costs due to poor implementations. Properly project the amount of human resources. Optimize and balance the[…..] […]
Read More…
PharmEng engineers are experienced in building scalable and robust pharmaceutical production facilities and processes while employing state of the art techniques to meet and exceed operational and regulatory requirements. Our experts have successfully completed facility and process engineering projects including; vaccine manufacturing, sterile manufacturing, oral solid and liquid dosage manufacturing, API manufacturing, medical device manufacturing,[…..] […]
Read More…
