Harrison's Tech Consultants

In HTC, We have been actively engaged in Regulatory, Auditing, Training and Site Development Services for Healthcare Industry. 

The scope of our consultancy includes :

1. Clinical Research Training and Education of Sites, Ethics Committees and In-house Clinical Research professionals

2. NABH and NABL consultancy for Nursing Homes, Hospitals, Laboratories, Health Care Units.

3. Site Development (Ethics Committee (EC) formation and Registration Support: This also includes EC formation, finalization of members, SOP development, Training of Members and Registration award at DCGI.
 
4. NABH EC Accreditation Support: This includes self assessment of EC functioning, SOP and documentation, support in submission of application, query handling and help address audit findings/CAPA etc. 

5. Inspection/Audit/Gap Analysis of Sponsor/CRO's in-house Operations, Vendor(s), EC and/or Sites

6. Regulatory Support: Support as a liaison at CDSCO and assist submission till closure of Clinical Trial/BA/BE applications.

7. Site Management- Resourcing, Management of Investigator Initiated as well mid scale commercial Clinical Trials( Device/Phased/Observational) across therapeutic Indications PAN India.

Executive Director

Cytespace Research Private Limited

Accountable for Quality output at Cytespace sites in North India.
Responsible to line manage SSEs, oversee their performance and manage the coordinate of study at sites.
Responsible for mentoring and grooming SSEs and Manager(s) within Cytespace.
To explore business opportunity(ies) within this region.

Been actively contributing towards Empowering Sites and ECs via knowledge and expertise sharing w.r.t latest regulatory updates, Essence of GCP, SOP writing and various case scenarios with solutions..

Also, actively working with corporate groups to train and guide the CRA and Project management team wrt various GCP and regulatory issues.

Senior Manager and Head of North Region

CLINIMINDS

Responsible for handling corporate GCP training and manage operations w.r.t training activities ( course as well as corporate) across all Cliniminds centers at a National level.

National Head-Training and Operations

ClinTec International

Successfully managed at team of 12+ CRAs and CTAs, Responsible for project deliverables, resource management and Business requirements of the organization.

Clinical Operations Manager

ICRI GROUP

Spearheaded Corporate Training Programmes in GCP/GLP/GMP for Pharmaceutical and Healthcare Industry

Associate Professor

Dabur India Limited

Responsible to perform trial site and process audits, development of department SOPs, Work instructions and impart SOP and GCP training to internal clinical research and DM team.

GCP Quality Incharge

Panacea Biotec

Perform in house as well as Site GCP Audits for phased trials PAN India. Support sites to accomplish successful Regulatory Inspections. 
Train CRAs on Technical and soft skills and enable them to improve their productivity and site engagement

GCP QA Auditor

CRA for Phase II, III and IV trials in Pain Management, Respiratory Illnesses, Diabetes and Anti infectives

Regional Clinical Research Associate

An M.Pharm (Pharmacology) by training with broad experience in Clinical Research. specializing in the areas of People and Line Management, Clinical Project Management, Training and Development, Operations, Clinical Study Set up (Phase I-IV), , Site ID and Development, GCP-Audits of Sites, EC  and vendor management.

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