Skip to content
Reghelps SRC
  • Home
  • About Us
  • Clinical Services
    Post Market Clinical Follow-Up

    Post Market Clinical Follow Up

    Medical Device Clinical Investigation

    Medical Device Clinical Investigation

    Medical Device Usability

    Medical device Usablity

    IVD Performance Evaluation

    IVD Performance Evaluation

  • Regulatory Services
    fda 510k

    US FDA 510(K)

    eu regulation

    MDR CE Marking

    ivdr ce marking

    IVDR CE Marking

    quality system

    Quality System

get in touch

EAR

India’s top choice for cost-effective clinical data collection and documentation services.India’s top choice for cost-effective clinical data collection and documentation services.

  • Do your firm provide UDI (Unique Device Identification) Support?

  • Product liability insurance under your service explain

  • How quickly can I appoint your company as my EC REP?

  • Can you help with Notified Body coordination or CE certification?

  • Will your EC REP name appear on my product label?

  • Is appointing an EC REP mandatory for CE marking?

Reghelps Src Icon

We combine technical precision with regulatory mastery to guide your medical device from concept to market—ensuring safety, effectiveness, and patient trust every step of the way.

Quick Links

  • Blog
  • Business News
  • Regulatory News
  • Career
  • Privacy Policy
  • Admin Login
  • Contact Us

Quote Request Form

  • Post Market Clinical Follow Up
  • Clinical Investigation / Trials
  • Usability/Human Factor Studies
  • Performance Evalaution
  • Clinical Evaluation
  • MDR CE Marking
  • IVDR CE Marking
  • FDA 510(k)

© 2025 • Reghelps SRC

Back to Top

Page load link
Reghelps SRC

Bangalore Office (Registered)

RegHelps SRC Private Limited

#303, Shakthi Mansion, 2nd Block,
Ramamurthy Nagar, Bengaluru 560016
P : +91 9705835637 / 7019031781

Delhi Office

51A, Pratap Nagar, Gali No 2, Mayur Vihar
Delhi – 110091
P : +91 9705835637

Email: info@reghelps.com

Go to Top