Agror Pharma is the state-of-the-art Cephalosporin manufacturing facility which started its operations in Islamabad, Pakistan having operational designs meeting USFDA, EMA, WHO cGMP standards. We are working in collaboration with InterNational Health and Clinical Research, Inc. (IHCR) USA (http://ihclinicalresearch.com) and as such leverages its scientific, quality, regulatory, and clinical expertise to bring quality products of international standards to market at affordable price. Agror Pharma is leading the way to get approval of its products by WHO, FDA, EMA for distribution in all regulated markets and to provide the same quality products to the people of Pakistan.
WHY AGROR?
Agror is a cGMP facility which follows international procedures, protocols, and controls for:
Qualification of laboratory and manufacturing equipment
Qualification of processes
Qualification and validation of analytical methods
Commissioning of facility
Quality Assurance and Documentation
CGMP & GLP PRACTICES
Agror’s quality assurance is demonstrated in all phases of a product’s manufacturing steps. Quality supervision begins at the test facilities of raw material with careful demonstration and general conduct of non-clinical safety. This ensures compliance with current Good Laboratory Practice (GLP) and consequently, the integrity of the data produced. Quality supervision then follows through, production and distribution, and concludes with shelf life surveillance.
OUR CODE OF CONDUCT & VALUES
Integrity, Trust & Collective Responsibility
Participative Management in Operations
Open Interpersonal Communication
Mentoring and Developing other Colleagues
Absolute Confidentiality
Continuous Improvement
Not hiring at the moment.
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