1. An Introduction to Advik Laboratories Ltd
Manufacturer & Exporter of
Quality Ethical & Generic Formulations

2. Company Profile
Advik Laboratories Limited (ALL) was incorporated on 9th September, 1994 as a public limited company. Later on it came out with the maiden public issue on 28th February, 1996.
The factory was set up in technical collaboration with PFC Pharma Focus, Switzerland. PFC is a worldwide recognized name in providing consultancy to the major pharmaceutical companies globally. Advik’s multi-category manufacturing plant has the flexibility to manufacture formulations of different therapeutic segments, in the form of Tablets, Capsules & Dry Syrups under the guidelines of ISO 9001:2008 & WHO-GMP certifications.
Advik is a professionally managed company with a team of highly qualified dedicated professionals to manufacture and promote the high quality medicines in various Indian and global markets.
With the growing market potential in Pharmaceuticals fields, we are striving ahead ethically towards providing high quality products for a better and healthier life.

3. Fact Sheet Industry Indian Pharmaceuticals – Formulations Business
Engaged in the Manufacture and Sale of Pharmaceutical Products in India and Abroad.
Listed
BSE & ASE
Registered Office
Delhi
Incorporation Year
1994
Manufacturing facility
A modern high quality production facility for Tablets, Capsules & Dry Syrups at Sohna Industrial Area, Haryana.
Built-up Area: 65,000 Sq Feet.

4. Why Us? Total Client Satisfaction Superior Quality Products
Premium & Tamper proof packaging
Large Production Capacity
Provide Customized formulation
Timely delivery and Competitive pricing
Transparent Business Transaction

5. Vision, Mission & Achievements
Vision: To be the provider of quality health services for the betterment of mankind.
Mission: To work towards the complete satisfaction of every customer through best in class quality products, competitive pricing, timely delivery and excellent service.
Achievement: Advik Laboratories is an ISO 9001:2000 certified company & WHO-GMP certified company. Advik believes in following the good manufacturing practices recommended by the World Health Organisation and constantly makes efforts to improve upon them.
In addition the company is undergoing expansion to meet the provisions of UK - MHRA. Advik Laboratories provides pharmaceutical formulations that matches the international standards of quality.

6. Product Profile
Advik is manufacturing Tablets, Capsules, and Dry Syrups under the following categories:
Antibiotics
Anti Ulcerants
Anti-Malarial
Anti-Cancer
Anti-Pyretic
Anti-histamines
Anti-inflammatory Analgesics
Analgesics
Anti Allergic & much more
Company has around 36 names of various products Registered under its own brand name like Admox, Mobitone, Breon, Zin-Ten, Carry-On etc to its Credit.

7. Production Capacity 10 Million Per Day TABLETS 3.6 Million Per Day
Advik has following capacity of manufacturing pharmaceutical formulations with latest machineries of WHO - GMP certification:
TABLETS
10 Million Per Day
CAPSULES
3.6 Million Per Day
DRY SYRUPS
60,000 Sachets Per Day
SVP as well as ointments & Liquid syrup
under consideration

8. Quality Inspection
Advik laboratories is equipped with the latest instruments for analysis and quality control. Stringent protocols are exercised to monitor various quality checks of raw materials, excipients, packing materials, semi-finished goods & finished goods.
The manufacturing processes & batch manufacturing methods are validated by an independent Quality Assurance Department. In addition we have elaborate Standard Operating Procedures for all our processes. Advik Laboratories has been set up from the ground level with the avowed objective of achieving USFDA standards of quality.

9. Infrastructure
We have “A” class most modern manufacturing facilities at
138, Roz - Ka – Meo, industrial Area, Sohna, Haryana
Constructed Area
65000 Sq. Ft.
Location
Just 30 Kms from Indira Gandhi International Airport, Delhi
We have installed Air-conditioning (AHU) & Clean Room System wherever required with 0.3 micron Hepa Filters.

10. Facilities
Demineralisation Water Plant: A multi bed demineralisation plant has been installed with RO and UV facility to provide demineralised water for the production process.
Steam: A boiler of 500 Kg/Hr is installed to provide steam to plant.
Air Conditioning & Environment Control: All the sections are provided with the separate air handling units with the Hepa filters to control upto 0.3 microns and maintain temperature & humidity in various areas of manufacturing & packaging under control.
Compressed-Air & Vacuum: An air compressor & vacuum pumps have been provided to the areas where required.
Electricity: We have been sanctioned 500KVA electrical load from Haryana State Electricity Board (DHBVN Ltd). In addition, the company has provided 285 to 500 KVA Diesel Generator set, so that power is available in the event of power failure. A separate 30 KVA genset has been provided for other services.

11. Finished Goods
All finished goods are tested as per specifications. We have made our specifications more stringent by introducing extra test and reducing certain limits prescribed in the various pharmacopoeia.
Only after the finished goods are approved by quality control department, they are released for packing. All packing lines are cleared and checked by in process supervisors, quality control personnel in order to ensure that previous batch is not left on the machine or conveyor. Packing is carried out as per standard procedures.

12. Thank You