ARIRDMSCRO IS YOUR RIGHT CHOICE IN ENSURING YOUR CLINICAL TRIALS REQUIREMENTS RIGHT, IN ALL PHASES OF DRUG AND/OR DEVICE DEVELOPMENT
We are a niche Indian start up Quality-Focused Clinical Research Organization. This is our commitment to bring medicines to patients faster through the provision of honest reporting in compliance to regulatory requirements, ICH-GCP, embarking on best quality driven clinical trials data capture, analysis and reporting.
Our Clinical Trials Services:
The clinical project manager is a professional who applies the definition of project management to the field of clinical research to ensure that all stages of a clinical trial are properly managed, that the objectives of the trial are
At ARIRDMSCRO clinical operations teams are responsible for designing, planning and physically running Phase I – IV clinical trials within the drug/ medical device discovery Project Management department.
At ARIRDMSCRO we believe in providing high quality clinical operations sites management, to support your drug/medical device development needs and to get drugs/medical devices to market as quickly as possible.
Our Clinical Trials Services:
- Secure a meeting with our team
- First execute a Confidentiality Agreement and/or Non-Disclosure Agreement
- Share your specifications for the proposed study
- Our Team will work internally to provide you the best solution to match your business need and partner with you on study. Post you either sign MSA or TORO or at least LOI.
Post agreement approval by both parties
- Based on our proposal acceptance, we share budget for study for approval with Client and post that plan and execute our Kick-off meeting with Client.
- ARIRDMSCRO optimally allocates its internal team resources to the assigned study, in accordance with client approval of internal resources credentials on CV.
- Project Management, prepares detailed Project Charter with Living PMP to be used in study
- Project Manager, in accordance with study sponsor, explains complete PMP with WBS to all participating teams or departments at ARIRDMSCRO
DrugDevice approval from regulator (Phase I - IV)
- With our internal management matrix, We ensure all your clinical trial data, abides by principal of ALCOA-C and meets our company integrity and quality. Ensuring round the clock improvement
- Ensuring compliance to applicable guidelines and regulations is successful
- Our Project Management team has successfully communicated and mitigated all study risks, thereby improving study efficiency and reduction in study timelines
- With this complete services, we combine with client to venture in new partnership, based on assured quality with trust and we continuously work internally on learnings from each study to harness our development and knowledge base for all future studies