Mickle has two WHO inspected multipurpose cGMP facilities at Himachal Pradesh in India. The Baddi (Himachal Pradesh) facility is also inspected by USFDA.

Baddi manufacturing site is located about 50 km north of Chandigarh on the Barotiwala Road, Baddi, Himachal Pradesh, India. The distance to the plant from Chandigarh city is 50 km.

The site is situated on a private industrial area spread across 8.07 acres of land. The total area of the site is 42,667.00 sq. meters with an existing built up area of 24000.20 sq. meters.

The site has a total of one multipurpose Production Blocks with dedicated manufacturing streams in each block. The blocks have been designed in a way that a single batch size as low as 2 kg & going up to 500 kg can be taken under cGMP environment.

The site is self- sufficient & has Pilot plant, Research & Development (R&D) Labs, Analytical Research & Development (AR&D) Lab, Quality Control (QC) Lab, Validation cell, Quality Assurance dept., Regulatory Affairs dept., Environment Labs besides Raw Material Stores, Finished Goods Stores, Utility Section, Liquid Material Storage and Effluent Treatment Plant (ETP).

The production blocks have multiple streams designed for the manufacturing and packaging of Pharmaceutical and Intermediates. Production Blocks are connected to the Clean Rooms which consist of Wet Milling, Drying (Fluid Bed Dryer [FBD], Tray Dryer [TD]), Rotary Cone Vacuum Drier (RCVD), Agitated Nutsche Filter Dryer(ANFD) Milling, Blending, Packing, Quarantine and Finished Good Storage areas. Its design meets the clean room ISO 8 class 100,000 standards and positive pressures are maintained as required. The air supplied is filtered through 10µm, 3µm and 0.3µm filters (HEPA) with minimum 30 air changes/hr. Micronizing facility is available at the site for particle sizing.

An intermediate production block for large volume products is available under cGMP environment. . The site has a centralized Quality Control Laboratory which is equipped with modern testing instruments and equipments. The Quality Control Lab is also supported with a well- equipped microbiological laboratory.

The site has a well-planned utility system which ensures regular supply of steam, electricity, filtered air, chilled water and purified water. The entire system is orderly placed to avoid cross contamination and mix-ups, and to meet the regulatory requirements.

The equipment installed allows a wide range of process variables in operation conforming to Current Good Manufacturing Practice (cGMP) requirements.

The Baddi site is inspected by US-FDA, European EMA, Korean FDA,WHO. The site is also certified for, ISO 9001:2008, ISO 14001:2004 & OHSAS 18001:2007.

The site has the following Accreditations - 

Mickle has two WHO inspected multipurpose cGMP Formulations and Advanced Intermediate manufacturing facilities at Derabassi, Nangal, Punjab in India. Besides the Derabassi facility is also inspected by European EMEA, Korean FDA.

Nangal manufacturing site is located at a large industrial township in Punjab, India (City/State/Country) which is about 250 km North of Nangal city on the national highway NH-8. The distance of the plant from Nangal railway station/town is around 5 km.

The site specializes in developing and manufacturing advance intermediates (KSM) with full regulatory support for our customers. All processes related to manufacturing of various drug intermediates involving chemical synthesis, isolation, purification, drying, milling, blending and packing, in process controls and testing by the quality control laboratory, etc. are carried out at this site.

The site has three manufacturing blocks, apart from Quality Control Laboratory, Raw Material Stores, Finished Goods Stores, Utility Section, Boiler Room and Effluent Treatment Plant (ETP). The production blocks have multiple streams designed for the manufacturing and packaging of Advanced Intermediates. Production Blocks are connected to the Clean Room which consists of Wet Milling, Drying (Fluid Bed Dryer [FBD], Tray Dryer [TD]), Milling, Blending, Packing, Quarantine and Finished Good Storage areas. The area is controlled under forced ventilation (VUS & VUE) with proper air filtration of 20µm, 10µm and 3µm with minimum 30 air changes/hr.

The site has a well-planned utility department which maintains regular supply of steam, electricity, cooling water, chilled water, D.M. water, vacuum, air, nitrogen, etc.

The entire system is orderly placed to avoid cross contamination and mix-ups, and to meet the regulatory requirements.

The equipment installed allows a wide range of process variables in operation conforming to Current Good Manufacturing Practice (cGMP) requirements.