Ashland, MA: MEDIcept Inc, a leading international quality and regulatory consulting firm focused on medical device and in-vitro diagnostics (IVD), and Reilly & Associates, a US-based privately held consulting firm specializing in medical device/biotechnology, announces the merger of the two companies.
The merger promotes the shared strategic goal of becoming a world-wide, leading quality and regulatory value-added service firm focusing on medical devices and medical technology. Together the joint firm offers the opportunity to more effectively serve their customers, ranging from start-up, virtual medical device manufacturers to Fortune 500 firms.
Both MEDIcept and Reilly & Associates share a common goal to positively impact medical device compliance and safety. This acquisition provides us with an opportunity to provide medical device manufacturers with value added services as they introduce devices into new markets.
According to F. David Rothkopf, President of MEDIcept, “Both MEDIcept and Reilly & Associates have common core values. We both aim to help start-up and pre-revenue medical device companies navigate the quality and regulatory environment, while assisting large multi-national device manufactures with efficient, tailored auditing and remediation advice.”
“Reilly & Associates is excited to become part of the MEDIcept team,” said Susan Reilly, President of Reilly & Associates, LLC. “This merger provides our ever growing client-base with an extensive network of experienced consultants to serve all of their quality and regulatory needs. As Reilly & Associates and MEDIcept have partnered in numerous projects in the past, the transitions to a single firm will be a simple one for all of our customers.”
We are committed to helping you find the most cost-effective method for achieving our client’s quality goals and regulatory compliance. Our role is determined entirely by your needs, and our objective is to dispense efficient and innovative solutions and assistance.
About MEDIcept:
MEDIcept strives to provide our clients with proven, trusted, and cost-effective solutions. We are an international consulting firm specializing in medical device, IVD, and biotechnology Regulatory, Quality, and Clinical Services. Since 1996, we have worked with thousands of companies to solve their most critical FDA and ISO issues. Our integrated solutions are rooted in our direct experience and span all stages of the product life.
About Reilly & Associates:
Reilly & Associates, LLC is committed to helping you find the most cost-effective method for achieving quality goals and regulatory compliance. Our role is determined entirely by your needs, and our objective is to dispense efficient and innovative solutions and assistance.