Congratulations to Tyler Anderson, who has been promoted from Life Sciences Recruiter to Lead Life Sciences Recruiter! This promotion is a testament to his hard work and dedication that he has shown in his time at Precision. Tyler has consistently exceeded expectations and consistently delivered results that has helped our candidates and clients to grow […]
Windham, NH – Precision Life Sciences announced today that Todd Marlin, AKA “The Quality Guy” has been promoted to the position of Director of Business Development. In his new role, Todd will now focus on building and establishing partnerships with emerging medical device, biotech and pharmaceutical companies across the country to help them fill their […]
Biomedical engineering is a rapidly growing field that combines the principles of engineering and biology to develop innovative solutions for healthcare challenges. From designing artificial organs to creating new medical imaging technologies, biomedical engineers are at the forefront of advancing medical research and improving patient outcomes. In this blog post, we will delve into the […]
Working with notified bodies during the development process of medical devices can be a complex and challenging task. Notified bodies are third-party organizations that are designated by a country’s regulatory body to conduct audits and certify that medical devices comply with the relevant regulations and standards. In order to successfully navigate the process of working […]
Audits are a staple part of life sciences companies such as pharmaceutical companies, medical or biologic device manufacturers, and many more in the industry, and are key to success. While an audit gives a company valuable feedback on the quality of their processes and products, failing an audit can have a range of consequences from […]
Life sciences is a vast and interdisciplinary field that encompasses a range of scientific disciplines that focus on the study of living organisms and their interactions with each other and their environment. Some of the key areas of study within life sciences include biology, biochemistry, genetics, and molecular biology. One of the main goals of […]
An FDA audit is inevitable for any organization that manufactures or processes medical equipment, devices or drugs. Once the inspector enters the building, it might leave your leadership and team members feeling one of two ways: A calm excitement for the prepared organizations that are prepared and ready to successfully go through the audit, or […]
View one or all of the 4-part med device development webinar series presented by Don DeLauder and hosted by Maria “Cristina” Muise, MBA, Ph.D., MBA, Ph.D. ABOUT THE PRESENTER: The webinars are presented by Don DeLauder. Mr. DeLauder is an expert in medical device development with over 25 years of experience in the field. He also has 14 […]
The medical device industry landscape of regulations is constantly changing. The European Union’s Medical Device Regulations (EU MDR) came into effect on 26 May 2021 after a three-year transition period, is no exception. The EU MDR (formally, EU MDR 2017/745) replaced the EU’s Medical Device Directive (93/42/EEC) and the EU’s Directive on active implantable medical devices […]
GMP audit
