Hilton Pharma has a state-of-the-art production facility designed to facilitate the production of the highest quality

products. This production facility is located at Karachi’s major industrial hub the Korangi Industrial Area. Hilton
Pharma adheres strictly to the principles of cGMP with its modernized production facilities, efficient production
control, quality assurance, industrial safety, occupational health and environmental control systems.
Raw materials are sourced from globally renowned manufacturers. These materials are subjected to a demanding
schedule for various testing procedures. Production of quality products at the manufacturing facility is approved
through regular inspections of local regulatory authorities and the principal companies whose products are
manufactured by Hilton Pharma under license.
At Hilton Pharma, quality management is our foremost concern because the company believes in building of
quality right from the selection of raw material through the whole manufacturing process, till the end product.
The qualitative edge of Hilton Pharma stems from our highly skilled work force and professional management
backed by an ongoing integrated human resource training and development program.
This in turn ensures that every product bearing the name of Hilton Pharma meets the highest international quality
standards of production, safety and efficacy, hence making the name of Hilton Pharma synonymous to ‘Quality’.
The ISO 9001:2000 and ISO 14001 certifications are testaments to the success of company’s quality management
systems.

Quality Policy
At Hilton Pharma, quality management is our foremost concern because the company believes in building of
quality right from the selection of raw material through the whole manufacturing process, till the end product.
The qualitative edge of Hilton Pharma stems from our highly skilled work force and professional management
backed by ongoing integrated human resource training and development program.

1. The Quality Policy of Hilton Pharma is designed to produce good quality medicines and make them
affordable to those in need.

2. At Hilton, it is a basic premise that Quality is not merely conformance to specifications; it is, in fact,

building quality into the product at all stages of manufacturing in order to achieve the desired results

within the required timeframe.

3. Hilton's quality system is based on the belief that there is always room for improvement and every

member contributes towards achieving the highest standards of quality.

Environmental Policy
Hilton Pharma’s Corporate Policy on Environmental Management System outlines an organizational framework for
systematic identification, control and improvement of environmental impacts and aspects. Elimination of all
possible pollutants and environmental hazards is ensured through an elaborate Environmental Policy. The salient
features of our policy are:-

a. Maintaining our plant, equipment and facilities in a manner so as to ensure a safe and clean environment.

b. Training our people with a view to creating awareness among them about the importance of a pollution-

free environment.

c. Maintaining a comprehensive Environmental Management System aimed at providing containment and

effective disposal of pollutants.

d. The company expects each of its employees to be conscious of the importance of a pollution-free

environment and contribute positively at the individual level in creating a pollution-free environment.

e. Pollutant waste is disposed of effectively through a process of proper incineration, recycling and

reduction.

f. Complying with regulations and environmental laws.

g. Measures for attainment of Environmental Policy objectives and goals.

At Getz Pharma, our new product development program generally includes pre-formulation
studies, excipient compatibility studies, analytical methods development and validation,
formulation development and optimization, formal stability studies, and manufacturing
process development according to ICH Guidelines. At Getz Pharma, we also have a quality
program dedicated to continuous improvement of product quality of running products at a
dedicated high-tech R&D site.
These laboratory-scale batches are subjected to stability as per the ICH norms. The
complete documentation of the laboratory data is presented in a format compliant with
European standards or in an FDA-compliant mode, depending on the targeted markets.
Getz Pharma also has research capabilities specializing in the design, testing and evaluation
of health care products for life sciences companies worldwide. Our technology development
team consists of scientists drawn from some of the best research organizations. Through a
combination of state-of-the art analytical instrumentation, infrastructure meeting global
development standards, and world-class expertise and level of scientific excellence, we
ensure that our clients receive true added value to their R&D projects, completed in the
speediest and most cost-effective manner without compromising data quality.
At Getz Pharma, we understand that a sound infrastructure meeting global standards is an
essential part of achieving our deliverables. Our laboratories are well-equipped to handle:
• Tablets, immediate release
• Tablets, controlled or sustained-release including MUPs
• Tablets, enteric coated
• Capsules, hard gelatin or HPMC, filled with powder, granules, mini tablets or pellets
• Capsules, controlled or sustained-release
• Oral liquids and suspensions
• Ocular drops, nasal sprays and inhalations
• Semi-solid dosage forms
• Injectable dosage forms including lyophilized products
• An ICH-compliant stability management program for testing stability