Next Gen Pharma India Pvt Ltd. is based in Delhi/NCR and operates as a distributor of pharmaceutical products. The company also provides clinical research and product development services in the area of probiotics.

CD Pharma India Pvt Ltd. is based in Delhi/NCR and operates as a distributor of pharmaceutical products. The company also provides clinical research and product development services in the area of probiotics.

KlinEra is a full-service clinical research organization with a mission to conduct ethical and efficient clinical trials that will accelerate delivery of novel therapeutic treatments to patients with quicker time-to-market for our clients.

 Coordinate & manage clinical operations and study team for conduct of successful trial (including submission of documents to Ethics committee,recruitment, informed consent process, sampling, scheduling visit, etc).  Monitoring completion, accuracy and filing of documents during the trial. Coordinating with sponsor monitoring (CRAs) during monitoring visits. Resolving online/off-line data queries. Responsibility related to submission of documents to Ethics committee… Show more  Coordinate & manage clinical operations and study team for conduct of successful trial (including submission of documents to Ethics committee,recruitment, informed consent process, sampling, scheduling visit, etc).  Monitoring completion, accuracy and filing of documents during the trial. Coordinating with sponsor monitoring (CRAs) during monitoring visits. Resolving online/off-line data queries. Responsibility related to submission of documents to Ethics committee, management of TMF and assistance to CRAs and monitors.  Handling of specific measurement equipment for various skin measurements. Responsible for developing and managing the patient database which includes recruiter network management, systematic patient coordination and scheduling. Show less

 Reviewing the protocol and other materials, such as the Investigator Brochure and informed consent form. Submission of study protocols and all pre-study documentation requirements to the ethics committee for approval.  Ensuring that all amended consent forms are appropriately implemented and signed. Scheduling Patient visit and follow up’s. Documentation of enrollment, medical report, follow up logs & case report forms. Investigational Product accountability and… Show more  Reviewing the protocol and other materials, such as the Investigator Brochure and informed consent form. Submission of study protocols and all pre-study documentation requirements to the ethics committee for approval.  Ensuring that all amended consent forms are appropriately implemented and signed. Scheduling Patient visit and follow up’s. Documentation of enrollment, medical report, follow up logs & case report forms. Investigational Product accountability and dispensing. Performing IVRS as per Protocol Requirement. Maintain study files on an ongoing basis to ensure that the files are complete and can be used as a source of reference. Coordinating with sponsor monitoring (CRAs) during monitoring visits. Resolving data queries. Show less