Experience

Getting a drug or medical device to market is a high stakes proposition. After investing many years and millions of dollars in research and development, minimizing the time and challenges of the approval process is critical.

Your consultant selection can affect the time it takes your product to reach the market. Our knowledge and experience from protocol design through final submission saves valuable time. Our sensitivity to your budgets and development costs conserves your resources.

Over the years, Ideal Consultancy Services has contributed to many FDA submissions that resulted in product approval for pharmaceutical and medical device companies. We bring a wealth of knowledge and experience to your project, working as a seamless extension of your team.

The table below summarizes the industries, therapeutic areas and project types with which we are experienced.

Industries

Pharmaceutical
Biotechnology
Medical Device
Medical Imaging

Therapeutic Areas		Project Types
Pharmaceuticals:	Medical Devices:
Cardiovascular (Imaging Agents & Therapies) Anti-viral Agents (HIV) CNS (Anticonvulsant, Neuromuscular Blockers, Pain) Oncology Respiratory Antibiotic Gastrointestinal Dermatology	Urinary Incontinence Stimulators Pain Studies ESW Therapy Spinal Implant Studies Stents Imaging Agents & Devices Diagnostics Hip Resurfacing	Animal Studies DSMB Consulting ISS/ISE Analyses Study Planning Phase I-IV Trials Medical Device Applications NDA, PMA, 510K Submissions Clinical Data Management FDA & EMEA Representation

SAS Training

Intro to SAS® System Course
SAS® Fundamentals Course
SAS® Programming Course
SAS® Report Writing Course
SAS® Advanced Techniques and Efficiencies Course
SAS® Macro Course
SAS® SQL Course
Using SAS/STAT® for Applied Statistics Course
Using SAS/GRAPH® Course