TRIANGLE REGULATORY PUBLISHING has experience in all aspects of regulatory publishing, including document formatting (MS Word and Adobe PDF), report and submission publishing, both for paper and electronic submissions.
We will provide exemplary service, custom tailored to fit the client’s needs. We are offering a wide array of options—from on site trainings of client employees to complete submission of client projects. Clients are able to choose the level of support they require from our “menu” to best accomplish their goals in a cost-effective manner.
Since the FDA is mandating the switch to electronic filing of documentation, many smaller pharmaceutical and biotechnology companies have been caught in a bind. With the cost of software alone running into the millions, the capital outlay to perform this work internally can be prohibitive. In addition, maintaining a personnel base with this skill set is complex, requiring regular retraining. This is currently leading some midsize and large companies to turn to outsourcing to fill these needs as well.
TRIANGLE REGULATORY PUBLISHING provides cost effective, quality solutions for all of your regulatory submissions needs.
TRIANGLE REGULATORY PUBLISHING is a pharmaceutical service start up based out of Durham, NC with four founding members. The members have between them, nearly 100 years experience in the Pharmaceutical Industry, within both small and larger pharmaceutical companies which will allow them to provide quality service in a timely and professional manner.
Please email us with any questions.
