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Why Us

Vaayath > Why Us
why choose us

Why Us ?

We are committed to delivering outstanding results, providing invaluable insights, and offering strategic support throughout the regulatory process. Our team is committed to delivering services in a timely and efficient manner, without compromising on quality. We strive to meet deadlines and ensure that our clients can navigate the regulatory process smoothly and efficiently. So Partner with Vaayath and experience excellence in pharma regulatory services. We are confident that our team at Vaayath will exceed your expectations and provide the necessary support and guidance to help you succeed in your regulatory endeavors. We look forward to the opportunity to work with you and contribute to your success in the pharmaceutical industry.

  • Comprehensive Regulatory Services
  • Trusted Expertise
  • Customized Solutions
  • Timely and Efficient Services
  • We guide or customers through the complete regulatory process, right from dossier preparation to filing to final approval.
  • We help our clients with product selection by providing the market data relevant to the product in question. This provides an insight and makes decision making easy for client to decide whether to move ahead or drop the project or may come up with modifications.
  • With a 100% success rate, we can be relied upon to handle your project with utmost sincerity.
  • We support our customers in preparing replies for the concerns raised by the authority on the CMC, clinical, non-clinical, administrative or any other issue.
  • We do not deliver on time; we actually deliver before time. With a strong team of experts, dedicated associates, we leave no stone unturned to get the projects approved before time.
  • Our support team aids in post marketing activities viz PSUR filing, PI updates, applicability of updated rules and guidelines on approved products etc.
  • Variation/ Post approval changes filing and their approval.
  • We upfront provide the checklist for various applications so that the client be better prepared beforehand. This helps to prepare the error free documentation and aids in expediting the filing process.
  • For new manufacturing set-ups we provide layouts meeting all the applicable GMP requires of USFDA, EU, PIC/s, WHO etc. We also help our clients to identify the right civil contractors, AHU suppliers, Water system suppliers etc.
  • We provide transparent guidance on the product and process related queries. We provide the complete pathway to our clients with probable timelines at each step, so an informed decision can be taken.
  • We support our client to identify the best service providers for all the allied services such as Clinical Research Organizations (CRO’s), Labs for non-clinical studies, RM suppliers etc. We only work with Govt. approved suppliers but also ensure that they are the ones with highest credibility and data generated is authentic and error free.
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