"Quality is an Endless Process. EASY GROUP is climbing the mountain, on top of which is Quality"
EASY GROUP Quality control department is equipped with the most modern analytical instruments complying to Good Laboratory Practices (GLP) which conduct the testing in accordance with the applicable pharmacopoeias monographs (BRITISH PHARMACOPEIA, US PHARMACOPEA).
At EASY GROUP, certified analysts carry out Raw MATERIAL , Packaging material analysis, Bulk and Finished Product analysis and review the batch documents beside performing environmental monitoring of the plant through Personnel swabs as well as surfaces swabs, MACHINE SWABS.
QC is responsible for sampling, testing and specifications and for the organization necessary to provide documented evidence that all materials and products are in compliance with pre-determined specifications and are suitable for their intended use.
EASY GROUP Quality Assurance system is designed so as to meet the most stringent regulatory requirements and surpass the industry standards in terms of Safety, Efficacy and Quality of the products.
EASY GROUP Quality Assurance (QA) system encompasses all current good manufacturing practices (cGMP's) including effective quality control (QC) as well as design and development considerations.
Among the QA noteworthy activities are self-inspections for cGMP compliance, deviation handling, corrective and preventive measures, handling of customer complaints and organizing product recalls (should they become necessary), coordinating documentation efforts, document control, finished product release, as well as supervising qualification and validation activities.
EASY GROUP also uses the expertise of internal & external consultants who carry out quality audits and advise us on the continuous improvement of EASY GROUP quality system.
EASY GROUP puts the Customer in its focal concern. To implement Policy, EASY GROUP views Quality to be ; not just complying to specifications, but satisfying customer needs for efficient, safe, and competitive products through :
-Devotion of the whole staff at various levels within the organization to Quality Standards.
-The Continual improvement, Training, and increasing self capabilities of Employees.
-Application of ISO Standards for Quality & Environmental Management Systems
EASY GROUP Company holds ISO 14001 (ENVIROMENTAL MANAGEMENT SYSTEM) . The Company Shares the Governmental efforts to protect the Environment. Through a declared Policy, EASY GROUP recognizes its responsibilities in :
Prevention of Pollution.
Complying with ethical and legal requirements.
EASY GROUP implements a series of measures to protect the Environment e.g.:-
Waste water is analysed routinely to assure its compliance with the regulatory requirements.
Procedures are set and implemented to assure Environmental protection during waste disposal.
Communicates with Official Environmental Parties.
Obtain Environmental Brochures, Circulars, & Journals to update its knowledge.
Prohibits smoking within Factory site.
EASY GROUP Company holds ISO 9001: 2008 (Quality MANGEMENT SYSTEM ).&ISO 18001:2007( OCCUPTIONAL HEALTH AND SAFETY MANGEMENT SYSTEM ) The Company applies cGMP in manufacturing its Products. Through a declared Policy, EASY GROUP recognizes its responsibilities in:
Manufacturing safe, effective, and highest Quality Products.
Implementing Procedures that guard against product contamination or mix-ups.
Considering the safety of the Employee & Product Safety in the Design of the Factory used Machinery and Training Programs.
EASY GROUP implements a series of measures to enforce the Safety of Employee and Product e.g.:-
Sampling and Dispensing Raw Materials under Safety Cabinets designed to protect Employees and Materials.
Manufacturing processes are performed in areas isolated completely from external environment.
Procedures are set and implemented to assure Employee / Product Safety during Handling and Manufacturing. Employees wear Safety tools during Manufacturing and Analyzing the Product.
EASY GROUP works with an Integrated Quality System, in which all Departments are responsible for the Quality of the end-product. A Quality Directorate is working within the Company to assure Quality is built into the product throughout the Manufacturing Chain, and compliance to specifications
Responsibilities of Quality Assurance Department:
Full compliance to Good Manufacturing Practice (cGMP) and Good Laboratory Practice (GLP)
Continuous in-process control & monitoring
Equipment, process and utilities validation
Vendors auditing and approval
Standard Operating Procedures.
Compliance to ISO 9001&14001 &18001 standards.
Continuous training and upgrading the knowledge of quality observance.
Internal Audit of the plant. |