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http://lotuslabs.com/en/regulatory-submission.aspx

These are the public entries for this link:

• Regulatory Submission
  The Regulatory Submission Teams at Lotus Labs are committed to ensuring best-in-class regulatory submissions with sound knowledge of regulatory requirements, international norms &interacting with global regulatory bodies enable us to ensure quality & reliable compliance with regards to study submissions. The regulatory submission activities include Formulation of regulatory strategies, Compilation of the clinical trial application, Submission and follow-up of the application, Response to regulatory agency queries, Procurement of drug import licenses, Procurement of NOC for export of biological samples and many more as required by the sponsor.
  By lillymark in Public bookmarks with regulatory regulatory-.--submissions submission
• State-of-the-Art Phase I Clinical Trial Facilities
  Lotus Labs has independent Phase I clinical trial facility & the expertise to conduct First-In-Human Studies, Pharmacokinetic studies, Bio-availability & Bio-equivalence studies, Drug Metabolism studies, Dose Proportionality & Multiple dose studies & more.
  By lillymark in Public bookmarks with 1 clinical i phase phase-i-clinical--trial trial trials

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