UNI-MED is privately owned leading pharmaceutical,
Diversified company
manufacturer of wide
Uni-Med is supplier of variety of pharmaceutical packaging material
(empty hard gelatin capsules,foils,caps)
Quality
“Quality is never an accident; it is always the result of intelligent efforts.”
Quality has always been an on going process which has brought the international standards closer, with the world appearing smaller. Each unit that is manufactured is guaranteed with a promise of Quality because of the total observation of the uniform standards that are used. In accordance with WHO-GMP and ISO 9001: 2000.
Our Quality Policy :
we shall strive to sell cost-effective pharmaceutical products and services that meet the needs of our international customers and of established Quality standards laid down.
Effective Quality Management system in accordance with WHO-GMP and ISO 9001: 2000
we shall strive to achieve market leadership in the defined area of our business activity
we shall in addition, constantly upgrade ourselves by way of knowledge, training and facilites. and employ CIP (continuous improvement process)
Provide growth opportunities to the organization and its stakeholders.
Quality Control
Quality is our strength and in order to maintain it at every stage of production we have inhouse most modern testing Laboratory equipped with all necessary hi-tech instruments and qualified technical staff. We operate in total compliance with the G.M.P norms set by the W.H.O. These norms are controlled by and a superior hi-tech quality control laboratory divided to three laboratories.
Chemical Laboratory.
Physical Laboratory.
Microbiological Laboratory
we have a sophisticated quality control Laboratory which carries out quality control,
R & D activities. and follows good laboratory practices and incorporates the most modern testing equipment, in order to perform the stringent quality analytical tests prescribed by different pharmacopoeia. Some of the modern equipments in our laboratory are H.P.L.C ., G.C. with Head space, stability chambers, TLC Chamber, UV Spectrophotometer, Polarity-meter for optical Resolution, Melting Point Apparatus, Karl Fischer Aperture etc. A quality control certificate is given with every batch material when supplied to our customer.
The Q.C. department is responsible for in-process Quality control activities, Finished
Product analysis and analysis of validation samples. Q.C dept exercises its control
from the start of any manufacturing process till the end of it.
Quality Assurance
“Quality is a journey, not a destination ….”
Vendor evaluation and selection is carried out as per stringent quality, product manufacturing, service and delivery parameters to ensure the highest quality raw materials that are used. There is a regular validations of process, test methods, water and environment, as well as periodic calibration of all instruments, to guarantee product output of top quality.
The Quality Assurance (QA) Department manned by qualified personnel, constantly monitors quality parameters – performing systematic sampling and testing at every stage from raw materials, through each process of intermediate and finished products.
QA Department also maintains detailed Batch Manufacturing records (BMR) on all products sold by us. These files hold the following pharmaceutical information :
Composition
Certification of Analysis.
Manufacturing records
Stability data.
Batch Manufacturing Records are prepared and issued by a technically competent person
for each planned batch. On completion of the batch all BMRs are sent to Quality Control
Department.
The proven efficacy and high shelf life of our products result from the painstaking efforts
we take in ensuring that only the best manufacturing practices are followed at every step.
