Our services

Clinical trials (Phase II - IV)

Our CRO has vast experience in conductiong Phase I - IV Clinical Trials across varieties of therapeutic areas.

 

Phase II – IV

Therapeutic areas

 

CRO offers knowledgeable and skillful Clinical Research Associates ( CRAs ) to monitor and administer clinical trials monitoring. Close out visits are managed as per sponsor’s requirement and reporting methods documented in the clinical monitoring plan. CRAs are well trained in GCP, SOP, technology, scientific and medical issues and are versed in industry development. Our CRAs work closely with sites to collect spotless data promptly. In case of requirement, we also place CRCs at sites.

 

STRENGTHS AND SKILLS

  1. Extensive network of hospitals and medical institutes throughout India
  2. GCP trained clinical trial monitoring team
  3. Well-defined SOPs to comply with GCP
  4. Database of investigators in diversified therapeutic area
  5. Collaborative work with the prestigious state research institutions for NCE

 

GCP trained clinical trial management team, with experience in various therapeutic areas, is backed by extensive network of hospitals and medical institutes thorough out India. With a large number of databases of investigators, Cadila CRO offers complete package for conducting phase II to III Clinical Trials. We also have collaboration with many prestigious Government Research Institute for NCEs.

 

SERVICES OFFERED

Medical WritingProtocol Development :

  1. Protocol Development 
  2. Expert review & reports of Safety data
  3. Regulatory Support
  4. ICF & CRF designing.
  5. Statistical analysis report

 

Site Development Investigators Management :

  1. Site & Investigators  Identification
  2. Investigator's training programs
  3. Medical monitoring and Query management
  4. Randomization, packaging, coding & labeling of Investigational Product's & site supplies
  5. Contracts with Investigators
  6. Site Initiation
  7. Study close out

 

Project Management & Site Monitoring :

  1. Clinical development plan         
  2. Quality systems Implementation
  3. SOP Management
  4. Clean & locked data and corrective measures management
  5. Meetings & Trainings.
  6. GCP Audits at sites.