Driving innovation & accelerating progress
From clinical trials to protocol development, data management and more – see how our services can meet your specific needs.






Clinical trials
TASK offers a full range of clinical trial services tailored to meet your specific needs as a pharmaceutical or biotechnology company. Our expertise spans from early-phase drug development to late-stage trials, ensuring rigorous adherence to regulatory standards and ethical guidelines. With a global network of experienced investigators and state-of-the-art facilities, TASK delivers efficient and reliable clinical research solutions, driving innovation and accelerating drug discovery.
Protocol development
TASK provides expert guidance and support to sponsors throughout the protocol development process, ensuring that the study design is scientifically sound, feasible, and aligns with regulatory requirements. Our experienced team can help with drafting, reviewing, and refining protocols to optimize data quality and minimize risks.
Data management
Our data services offer comprehensive solutions to support sponsors throughout the clinical trial lifecycle. Our team can help with the following data services:
- CRF Design
- Database Design
- Database Validation
- Data Management Plan
- Data Entry
- Data Cleaning
- Pharmacovigilance
- Database Lock & Transfer
- Statistical Analysis Plan
- Statistical Analysis
Regulatory services
TASK’s regulatory expertise ensures seamless compliance with global regulatory standards and guidelines.
Our team can provide:
- all aspects of regulatory and ethics submissions
- protocol amendment submissions and processes
- informed consent drafts and reviews
- clinical trial registration (SANCTR/PACTR/CLINICALTRIALS.GOV)
- investigator site file set up and maintenance training and services
- sponsor trial master file set up and maintenance training
- regulatory workshops for new sites or regulatory staff
BSL-3 laboratory
Our dedicated biosafety level 3 (BSL-3/P-3) mycobacteriology laboratory specializes in providing:
- high quality microbiology research and diagnostic services
- mycobacterial quantification
- drug sensitivity testing
- PBMC isolation
- cryopreservation
International accredited training academy
We believe capacity is built by reimagining the way skills are traditionally taught to clinical research staff. Our teaching methodology involves learners in experience-driven environments where they can immerse themselves in the world of clinical trials and learn what to do and why to do something – at every stage of the clinical trial process.
As a result, teams partnering with us will be learning from the best to become the best, because we believe in developing tomorrow’s clinical research professionals today. Learn more about our courses here:
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01
Clinical trials
TASK offers a full range of clinical trial services tailored to meet your specific needs as a pharmaceutical or biotechnology company. Our expertise spans from early-phase drug development to late-stage trials, ensuring rigorous adherence to regulatory standards and ethical guidelines. With a global network of experienced investigators and state-of-the-art facilities, TASK delivers efficient and reliable clinical research solutions, driving innovation and accelerating drug discovery.
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02
Protocol development
TASK provides expert guidance and support to sponsors throughout the protocol development process, ensuring that the study design is scientifically sound, feasible, and aligns with regulatory requirements. Our experienced team can help with drafting, reviewing, and refining protocols to optimize data quality and minimize risks.
-
03
Data management
Our data services offer comprehensive solutions to support sponsors throughout the clinical trial lifecycle. Our team can help with the following data services:
- CRF Design
- Database Design
- Database Validation
- Data Management Plan
- Data Entry
- Data Cleaning
- Pharmacovigilance
- Database Lock & Transfer
- Statistical Analysis Plan
- Statistical Analysis
-
04
Regulatory services
TASK’s regulatory expertise ensures seamless compliance with global regulatory standards and guidelines.
Our team can provide:
- all aspects of regulatory and ethics submissions
- protocol amendment submissions and processes
- informed consent drafts and reviews
- clinical trial registration (SANCTR/PACTR/CLINICALTRIALS.GOV)
- investigator site file set up and maintenance training and services
- sponsor trial master file set up and maintenance training
- regulatory workshops for new sites or regulatory staff
-
05
BSL-3 laboratory
Our dedicated biosafety level 3 (BSL-3/P-3) mycobacteriology laboratory specializes in providing:
- high quality microbiology research and diagnostic services
- mycobacterial quantification
- drug sensitivity testing
- PBMC isolation
- cryopreservation
-
06
International accredited training academy
We believe capacity is built by reimagining the way skills are traditionally taught to clinical research staff. Our teaching methodology involves learners in experience-driven environments where they can immerse themselves in the world of clinical trials and learn what to do and why to do something – at every stage of the clinical trial process.
As a result, teams partnering with us will be learning from the best to become the best, because we believe in developing tomorrow’s clinical research professionals today. Learn more about our courses here:

Learn more about our therapeutic areas
Therapeutic Areas