We have ambitious future plans for the growth of our business as well as for the benefit..
Our Vision is to provide world class, cost-effective products for the international as well as domestic market reuirement..
We have constructed a modernized infrastructure unit to maintain smooth functioning of business activities.
Ever since our organization has been incepted, we have given utmost importance to the quality standards of the products.
Established in 1981, over the last 20 years Lanz Labs has made progress by leaps and bounds and is today a leading Pharmaceutical company in the area of Health Care, manufacturing Bulk Drugs & Drug Intermediates.
Our factory, which is situated at a distance of about 30 kilometers from Bombay, has a finishing section, namely Pharma Zone, which is provided with Air Conditioning using filtered air through a dedicated air handling unit. The in-house utility facilitates such as Steam, Electricity, Water, Chilled water, and Demineralised water. The company has generators for additional power supply. The facilities provided are well-maintained at all times with prompt and adequate repairs.
Lanz Labs has adopted a policy of operating the pharmaceutical manufacturing under the control of a Quality Management system.
Quality Control is empowered to ensure that all strict measures/standards which are legal as well as jointly set by the customer and our company are adhered and followed from manufacturing to finishing and dispatching. It is also our policy to update the standards as per cGMP and customer requirements by means of mutual dialogue.
The quality control department is full authorized to take appropriate decisions on quality matter.
With a view to maintain quality of our products in Lanz Labs all procedures are written in detail duly authorised for all operations including Manufacturing, Analysis, Material Management, Distribution, Environment Controls, Housekeeping, Sanitation, Health and Hygiene and Engineering.
Quality control system comprises of checking of all incoming materials, independent overseeing of all processes and examining of Finished products, documentation and system of complete docket/process checks before actual products are released for sale.
Semi-finished and finished products are released for packing and for sale respectively by Quality Control. Samples of each batch of each product are drawn by QC as per the sampling program. Complete analysis is done as per the release specifications (Pharmacopoeia or In-House). Results are recorded in test protocols and reports.
Quality Control is well equipped with important analytical instruments such as:
GC
HPLC
FTIR
UV SPECTROPHOTOMETER
POLARIMETER
KARL-FISCHER TITRATOR
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