About Us


Micro Labs

Quality is one of the core philosophies at Micro Labs. Stringent quality measures are applied to the manufacturing process of each product. Our reputation as a leader in the pharmaceutical business has been established due to our dedication towards maintaining the highest of quality standards. Quality guidelines practiced at Micro Labs include.


    Creating intelligent product design


    Utilize the best available resource


    GMP–compliant manufacturing facilities that meet requirements of all leading regulatory agencies of the world such as US FDA, UK MHRA, ANVISA Brazil, WHO


    Recruitment of qualified and competitive professionals

Our efforts at producing the best pharmaceutical products have been duly recognized by IDMA (Indian Drug Manufacturing Association) and the company has won 3 awards in 2009, 4 awards in 2010, a clean hat-trick of 3 awards in 2011 and an unprecedented 4 awards in 2012 and 1 award in 2015.

Micro labs Baddi Plant was bestowed with Quality Excellence Gold Awards in 2012, 2013 and 2014 by India Manufacturing Excellence Awards (IMEA) conceptualized by Frost & Sullivan in association with Economic Times.

Micro Labs Sikkim Plant was recently awarded with  Quality excellence Silver Award  by  Indian Drug Manufacturers Association ( IDMA) in 2015

Micro Labs has adopted Quality Systems & Based approach for implementation of Good Manufacturing Practices and continual improvement. Therefore, at Micro Labs, Quality is a way of life.


  • Report adverse experiences with medications
  • Report serious adverse reactions. A reaction is serious when the patient outcome is:
    • Death
    • Life-threatening (real risk of dying)
    • Hospitalization (initial or prolonged)
    • Disability (significant, persistent or permanent)
    • Congenital anomaly
    • Required intervention to prevent permanent impairment or damage
  • Report even if:
    • You’re not certain the product caused adverse reaction
    • You don’t have all the details however point nos. 1, 5, 7, 8, 11, 15, 16 & 18 (see reverse) are essentially required.
  • Who can report:
    • Any health care professional (Doctors including Dentists, Nurses and Pharmacists).
  • Where to report:
    • After completing, please return this form to Micro Labs Ltd, Pharmacovigilance Cell
  • What happens to the submitted information:
    • Information provided in this form is handled in strict confidence. PV cell at Micro Labs will carry out causality analysis and the data is statistically analysed and finally submitted to CDSCO.


The patient’s identity is held in strict confidence and protected to the fullest extent. Programme staff is not expected to and will not disclose the reporter’s identity in response to a request from the public. Submission of a report does not constitute an admission that medical personnel or manufacturer or the product caused or contributed to the reaction.