Regulatory ServicesRegulatory submissions and reporting to global authorities. Review of IFUs, signal investigations, and risk assessments. Development of clinical evidence reports.
CRO Services LAAN Research offers a wide variety of clinical trial and safety services for pharmaceutical and medical device manufactures.
Pharmaceutical & Device Development LAAN Research has experience in every aspect of Clinical Trial Development, everything from initial protocol writing all the way through to post marketing trials.
LAAN Research provides complete clinical safety services, including CEC member selection, organization of the consulting agreements, management of CEC meetings and coordination of the entire adjudication process.
MedDRA Coding Services
The coding of adverse event (AE) terms using the Medical Dictionary for Regulatory Activities (MedDRA) can be a challenging task for most organizations.
LAAN Research has supported sponsors with DSMB work on more than 50 studies with a variety of products. We have access to a pool of practicing physicians who are well versed in the safety oversight of clinical trials for a broad range of therapeutic areas.