Phase IV

Assistance for Every Phase of Pharmaceutical Research
When it comes to introducing (or re-introducing) a new pharmaceutical or device, obtaining regulatory approval is just the beginning. The market must be developed, and that requires an expert strategy plus timely implementation.

Whether your research and development effort requires an assistant, an advisor, or a full partner, Beardsworth has the resources and experience necessary to make your plans a reality. We provide clinical research management, data management, quality assurance, and medical writing to pharmaceutical, device, and biotechnology companies throughout the nation.

In the Beginning
Market development begins with post-approval clinical testing. Highly focused, and easy to carry out, post-approval testing increases usage among current customers and initiates it among new ones. Sales grow, market share expands, plus you build a valuable database of results that can be used to showcase product benefits. Depending on design, post-approval studies can also be used to revise advertising and initiate new labeling.

Beardsworth Delivers Quick, Cost-Efficient Results
Beardsworth personnel are experienced in every stage of pharmaceutical research and development, and can provide as much or as little support as you need. We can manage post-approval studies from start to finish, and then design a strategy for presenting the findings at professional meetings, dinner symposia, and in peer-reviewed journals. If desired, Beardsworth can advise you in pursuing additional regulatory approvals.

Our experience in clinical research management means that we avoid common difficulties that can delay or invalidate results. The keys to post-approval clinical trial success include:

• targeted physician selection
• clear instructions
• focused parameters
• timely completion
• an experienced study management team
• exacting data collection and reporting

Beardsworth can design your protocol, ensuring that it is focused and easy to follow. Contact with the physicians, simple protocol design, and vigilant data management ensure the success of your trial.

What's in it for our Clients
Done right, post-approval clinical trials help build usage of your product among current customers and encourages its use among new, high-potential customers.

What can you expect from Beardsworth? A very experienced CRO that does work for their clients not make work. And at the same time be a partner who will maintain an unwavering commitment to your goals.

For details on how Beardsworth can support your product development and marketing goals, call either: Michael O'Brien at (908) 788-1729 or e-mail him at .