Milan Laboratories (India) Pvt. Ltd. was establshed in the year 1976 with the objective of manufacturing pharmaceutical formulations. A modest beginning, while being morally obligated towards improved human health, liquid orals and tablets were manufactured for the local markets. Supported by the initial success, other dosage forms such as capsules, dry syrups and Ointments were also added. The gradual expansion of the organisation was a series of milestones over the years which included Exports, building of a separate facility for Penicillin antibiotics and a brand new facility for General products, all replete with modern, state of the art and most current cGMP compliant systems.

The latest cGMP norms were always adopted as a habit and culture. A qualified, experienced, continually updated and committed personnel base and our well maintained facilities has enabled us to achieve Quality certifications from WHO, UK-MHRA, South Africa-MCC, most other African and European nations.

Our Organisation is ISO 9001-2008 certified as well.

The organisation has been awarded Export awards from Chemexcil(Pharmexcil), FICCI and FIEO. The company enjoys star export house status.

Our Customer retention and satisfaction index speaks for our success so far.

Continual improvement is our policy and the company has been adapting to current trends and requirements while adding newer approvals and opening newer markets for business.


vision-2015-Milan-Laboratories

Our Mission


“To maintain our reputation as a quality conscious organization with strong ethical values as we keep growing and upgrading consistently”


Our Vision


“To achieve success in all regulatory approvals by building & maintaining strong systems”


1976: Establishment of the company with a liquid orals Section

1984: Commissioning of Tablet Section

2001: Commissioning of Semisolids Section

2008: U.K. MHRA approval

2011: Pharmaceutical GMP Services

timeline-Milan-Laboratories

1977: Start of Capsule Section

1996: Started with our own Export

2004 – 05: Establishment of New Penicillin Manufacturing Facility

2009: South Africa MCC Approval / Expansion of Penicillin Plant to include Dry Syrup and Tablet section.

2012: Commisioning of General Plant -2 as per EU – GMP Standards


M. M. Deshpande

Founder Member & CEO


Board of Directors


Upendra Deshpande

Director

Rohini Dongre

Director


Corporate Team

Sharwari Deshpande

Head of Quality Operations

Laxman Bhopi

Personnel Manager

Rajaram Jadhav

Production Manager

Megha Hajirnis

Chief Financial Officer

Sanjay Potdar

Production Coordinator

Rahul Dongre

General Manager

Quality Control

The Quality Control section is well equipped with professionals operating Qualified instruments for performing analysis of incoming materials, in process and finished products. This section is responsible for sampling, testing and release of materials at every stage of manufacturing.

 The plants are inspected by the Drug Regulatory Authorities / Health Authorities of various countries and the constant efforts by the Quality Operations cell has enabled us to have a very good success rate so far with renewed and valid registrations in several countries.

Quality Operations

The Quality Operations team at Milan Laboratories ensures to provide drugs of consistent quality, purity and efficacy to our patients. In order to achieve this, in house cGMP inspectors ensure that all activities in the manufacturing units are carried out in accordance with cGMP norms. In process controls, usage of qualified machinery, validated manufacturing processes, validated cleaning procedures, strict environmental & microbiological controls in production and packaging areas, training of personnel, maintaining hygiene and cleanliness, proper record keeping, and so on are some of the controls exercised by this section so as to ensure that Quality is built into the final product.

Key Quality Certifications

At Milan Laboratories, importance is always given to developing technology and manufacturing standards at all times. All our manufacturing facilities conform to WHO-cGMP standards & the products are manufactured under strict quality norms.

 

All interior partitions are done with integrated clean room modular paneling systems and atmospheric conditions being controlled by HVAC systems. All core process areas are supplied with air that is filtered through EU-13 Type HEPA filters.

Upcoming Manufacturing Facility

We are presently expanding and building a new manufacturing facility to cater to the regulated markets – USA and UK
This fully integrated state-of-the-art manufacturing plant is situated at Dahej (Guajarat), in an area of 37664 Sq. Mt.
The facility will be dedicated for Oral solid dosage forms