Synchron was started by a group of pharmaceutical professionals in 1998. Today Synchron is a leading Contract Research Organization in India providing broad range of clinical research services from phase I to phase IV, including :
- Bioavailability/bioequivalence
- Pharmacokinetic/Pharmacodynamic studies
- Dermatopharmacokinetics
- Bioanalysis
- Statistical analysis and Data Management
- Pharmacovigilance
- strictly adhering to ICH and GCP guidelines and other applicable guidelines and regulations.
Our Resources
At Synchron, the sponsor is supported by our highly skilled, full time trained professionals committed to provide the highest Quality Service. Synchron’s personnel have a totally scientific approach, are highly professional and committed with good knowledge and training in GCP/GLP.
To ensure the best Quality Services to our clients, we employ highly qualified and experienced staff. To maintain our high quality standards we continuously review our quality systems. Synchron’s training is a continuous process throughout the tenure of all the staff members.
Synchron is proud to provide its services to the industry with complete recognition of the importance of the quality of services and quality of relationship.
Our Commitment
Our staff is involved in projects from inception to completion. At Synchron our clinical trials are strategically planned and carefully implemented. Once initiated our ongoing system of continuous quality management is designed to identify issues early, implement corrective action and maintain oversight throughout the process in order to complete the study on time and within budget. Synchron functions with a set of detailed Standard Operating Procedures (SOP’s) for all Phase I-IV clinical trials and Data management activities. Data management operations are completely validated as per the regulatory requirements.