Book A Consultation
Book A Consultation

About Us

DQR MedTech Provides Services and Solutions to Support the Life Sciences Industry with Regulatory Affairs Operations and Strategy. As regulatory specialists, we work across all phases of the product lifecycle from regulatory strategy, authoring, and all aspects of established product maintenance, including submission management, publishing, and health authority interaction. We leverage a global team of consultants to provide local regulatory insight, strategy, and intelligence.
  • Our Mission
A reputable regulatory & quality organization known for serving its client’s best interests and solving their most difficult problems, by offering expert guidance and unbiased assistance.
  • Our Vision
To offer services worldwide and assist our client’s in getting the approvals of their breakthrough innovations. To solve documentation & traceability issues proactively.
  • Our Mission
A reputable regulatory & quality organization known for serving its client’s best interests and solving their most difficult problems, by offering expert guidance and unbiased assistance.
  • Our Vision
To offer services worldwide and assist our client’s in getting the approvals of their breakthrough innovations. To solve documentation & traceability issues proactively.

Company Profile

What We Do?

We help companies prepare documentation, review reports, perform risk analysis, and get regulatory approvals. We establish GCP, FDA, ISO, and applicable norms compliant pre and post market systems.

Read More

How We Do It?

We leverage expertise, use cutting-edge tools for project management and effective communication; pre-emptively informing about potential issues with an impact on cost and timeline.

Read More

Why We Do It?

We believe that safe and effective innovation should be aptly positioned to the regulators for timely approvals and continually made available to the patients and practitioners.

Read More

Our Core Values

Client Trust

We constantly strive towards earning our Client’s trust and delivering value

Accountability

We take responsibility for our actions and work towards constantly learning from our experiences

Innovation

We believe in constantly innovating in areas of technology and solutions.

Integrity

We strive towards high levels of excellence through integrity in every action we take and every commitment we make

Positive Work Culture

We believe in creating a conducive and positive environment at work

Transparency

We believe in providing our stakeholders the confidence and security that they deserve, by being transparent and open in our communications

Teamwork

We believe in working together collaboratively through sharing, caring and bonding.

Flexibility

We always listen to our clients’ needs and aspirations and based on this we are developing customized and efficient solutions.

Testimonials

I am very pleased to recommend Girish Hirpara. I have worked with him on freelance basis over past two years. Though I have communicated with him over phone, mails, and virtual media yet I have known him/her as a competent professional with solid knowledge of EUMDR, CER, CEP, BER, BEP and excellent work ethics.

I got a chance to engage him since last two years to till date whenever we have an urgent priority task on CER, CEP, BER, and BEP. He offered to complete the task at the earliest and it was completed as promised. He has a strong sense of responsibility and attention to detail which helps our company to enhance its customer base due to the quality of work provided.

He has been a great talent within our team as on requirement basis. I have seen him grow as an excellent employee. I highly appreciate/recommend for him for his skills that can be utilized for long-term in our organization.
Quality Representative/Person Responsible for regulatory compliances (Nemera SZC)
I have collaborated with Girish Hirpara on several projects for 2017/745, the EU Medical Device Regulations. Mr. Hirpara completed Clinical Evaluation Reviews, Biological Risk Plans/Evaluations and Post Market Surveillance for four (4) of our product families. Mr. Hirpara is knowledgeable of the requirements and brings a practical understanding of the regulations, at a reasonable price point. We continue to engage Mr. Hirpara as we seek to bring additional products to the EU marketspace.
Director RA/QA (North American Rescue Inc.)
I am very pleased to recommend Girish Hirpara. I have worked with him on freelance basis over past two years. Though I have communicated with him over phone, mails, and virtual media yet I have known him/her as a competent professional with solid knowledge of EUMDR, CER, CEP, BER, BEP and excellent work ethics.

I got a chance to engage him since last two years to till date whenever we have an urgent priority task on CER, CEP, BER, and BEP. He offered to complete the task at the earliest and it was completed as promised. He has a strong sense of responsibility and attention to detail which helps our company to enhance its customer base due to the quality of work provided.

He has been a great talent within our team as on requirement basis. I have seen him grow as an excellent employee. I highly appreciate/recommend for him for his skills that can be utilized for long-term in our organization.
Quality Representative/Person Responsible for regulatory compliances (Nemera SZC)
I am very pleased to recommend Girish Hirpara. I have worked with him on freelance basis over past two years. Though I have communicated with him over phone, mails, and virtual media yet I have known him/her as a competent professional with solid knowledge of EUMDR, CER, CEP, BER, BEP and excellent work ethics.

I got a chance to engage him since last two years to till date whenever we have an urgent priority task on CER, CEP, BER, and BEP. He offered to complete the task at the earliest and it was completed as promised. He has a strong sense of responsibility and attention to detail which helps our company to enhance its customer base due to the quality of work provided.

He has been a great talent within our team as on requirement basis. I have seen him grow as an excellent employee. I highly appreciate/recommend for him for his skills that can be utilized for long-term in our organization.
Quality Representative/Person Responsible for regulatory compliances (Nemera SZC)
I have collaborated with Girish Hirpara on several projects for 2017/745, the EU Medical Device Regulations. Mr. Hirpara completed Clinical Evaluation Reviews, Biological Risk Plans/Evaluations and Post Market Surveillance for four (4) of our product families. Mr. Hirpara is knowledgeable of the requirements and brings a practical understanding of the regulations, at a reasonable price point. We continue to engage Mr. Hirpara as we seek to bring additional products to the EU marketspace.
Director RA/QA (North American Rescue Inc.)
Previous
Next

Our Team

John Doe

Founder & Director

John Doe

Founder & Director

John Doe

Founder & Director

We deliver excellent service and provide experienced qualified personnel to strategically manage all aspects of your clinical trials.

Quick Links

Services

Contact Info

© 2023 DQR MedTech Consulting LLC. All rights reserved

Book A Consultation