Investigator’s Drug Brochure prepared specific to Natural Products.

Specialized Protocol writing skills.

Efficient Case Report Forms to allow Audit Trail.

Multilingual Consent Forms, high respect for Patient Safety and Rights.

Thoughtful Statistical Planning leading to achievable endpoints.

Efficient and well documented Trial Supply Management.

Elaborate Site Selection, Site Initiation and Investigators’ Meets.

GCP Trained, Experienced Investigators

Compliance monitoring by highly motivated and trained monitors

Timely Adverse Event and Serious Adverse Event Reporting

Direct Access to all site data allowing smooth GCP audit

Certified Central and Local Pathology Labs

Data Management using Clinical Oracle, Symetric or DMSys.

Statistical Analysis using SPSS or SAS.

Medical writing by joint team of investigators, medical writers from multiple disciplines

Prompt and accurate Interim and Final Reporting

No fault Clinical Trial Insurance cover

SOPs to ensure a QA System for Trial conduct and Data management

Manuscript writing and publication of study results

Reliable and safe Archiving

Non-comparator Dose Determination Studies (Phase IIa)

Double Blind Randomized Controlled Proof of Concept Trials (Phase IIb)

Healthy volunteer Cosmetology or Personal care studies

Multi-centric Phase III Studies

Safety Studies

Special age group, special population studies