We enable compliance, reputation and new growth opportunities for our clients

Welcome to Global Tech International-Medical Device
Consultancy

We are an organization of regulatory consultants for medical devices

Global Tech was founded in 2008 with a mission to empower the medical device manufacturers to comply with national and international regulatory requirements and boost up their businesses. Since then, GTI has worked with more than 60 national and international clients.

We offer a full range of regulatory services from the initial regulatory
strategy right through to approval and the post market phase. Our
insight into regulatory requirements will pave the way to a smoother
route to market.

ABOUT US

Who are we?

We are a consultancy company dedicated to medical device sector. Keeping in view the diverse challenges faced by people in this sector along with the constant struggle to ensure compliance and deliver safe product, we try to meet those challenges and provide best services to our clients ensuring compliance and solving regulatory issues.

WHAT WE CAN DO?

We provide full range of services required by medical device manufacturers and create value for our clients. Our services include: validations, management system, medical device files, product and process development etc. For further information about our services, view our SERVICE tab.

WHY CHOOSE US?

At GTI, we have an expert team who possess years of experience along with required knowledge. We believe in our capabilities and can translate our knowledge and experience to create value for you. . .

Team / Experts

MR. IMRAN GOYARA

Director

MR. SOHAIL GOYARA

Tax Consultant

IMRAN YOUSAF

Senior Consultant

MS. SAMMIRA

Regulatory Consultant

We are a specialist medical device consultancy consisting of industry experts with long and successful track records in commercialising medical device products. We have broad functional and sector experience, and would welcome an opportunity to discuss with you any challenge relating to creating sustainable value from medical technologies.

Latest News

VIEW ALL

Usability Engineering For Medical Devices
Usability engineering- also known as human factors engineering- is focused on designing medical...
Ethylene Oxide: Validation Process Overview
ETO is a colorless gas that is flammable and explosive. The four essential parameters (operatio...
Key Requirements of MDR
On April 5, 2017, the EU adopted the Medical Device Regulation, replacing the two existing dire...