Consultant Cambridge Regulatory. We have a network of ethical and high energy professionals with exceptional interpersonal, communication and leadership skills dedicated to help pharmaceutical companies worldwide to gain approval for their medicines in a timely and cost-effective manner with excellent organization and communication skills. Experienced in all phases of drug development and electronic and paper submission publishing, eCTD and CTD document processing, program management, legacy document processing, and archiving. We are providing support to many clients with regulatory strategy, quality assurance, CMC, Clinical, Operations and Publishing Submission Support. We manage all type of Regulatory electronic Submissions (eCTD) and hard-copy submission (CTD) the many global heath agencies. We have extensive experience helping pharmaceutical companies worldwide to gain approval for their medicines in a timely and cost-effective manner with excellent organization and communication skills.