Established in 2018, today, Concept Pharma Projects is one of the leading consultants for Pharmaceutical projects and also GMP consultant in India. Headquartered in Ahmedabad (Gujarat) and has an emphatic presence across the India with a wide repertoire as diverse as the great culture of the India’s healthcare system. CPP has aim to grown by leaps and bounds over the years in future.
About Us
Our Vision
We aim to be the most competitive and the most productive service organization in the world. Our core competencies in Pharma green field projects (turnkey projects), GMP projects, third party vendor audit and Regulatory services are being continuously improved to be best-in-class. They are at the heart of what we are.
Overview
Concept pharma projects (CPP) is a knowledge based, fully professional firm providing state of art solutions to clients throughout India, satisfying the local and regulatory GMP requirements.
CPP is a team of highly experienced and motivated professionals from the field of Quality assurance, quality control and engineering with hands on experience and technical expertise.
Since 2018, CPP has been offering one-stop Engineering Solutions to Finished Dosage Forms (OSD, Semi Solids, and Aseptic Products.),APIs, Analytical and Microbiological Laboratories.
Our Values
We seek to be characterized by our passion, integrity, entrepreneurialism and our innovative spirit, as we continually strive to fulfill our vision. These values guide us in all that we do and are the bedrock upon which our organization is built.
Strong emphasis on Transparency and Confidentiality
CPP’s services are underpinned by superior quality standards, attention to detail and longstanding relationships with our clients. Concept pharma projects is dedicated to conducting its work in a transparent manner to ensure that activities are always ethical, and that there is never a conflict of interest.
Equally, CPP understands the importance of confidentiality and treat the information our clients share with complete discretion. CPP’s confidentiality agreements are in place to protect clients as well as other stakeholders including the general public. The highest ethical and confidentiality standards are maintained at all times.
The audit reports CPP produces are strictly confidential and they are not provided without the express permission of the supplier. The details of the projects are provided within the limits of confidentiality.
Our Expertise
As a consultancy services, CPP is dedicated to supporting the pharmaceutical industry by sharing our knowledge and expertise. Most of our consultants have 10 to 25 years of experience in the pharmaceutical industry in areas such as Quality Assurance, Regulatory Affairs, pharma engineering, Process Development and Pharmaceutical compliance.
CPP’s growth and success would not be possible without the hard work and commitment of our team. Our highly experienced pharmaceutical consultants are committed to providing measurable and added value services on a worldwide basis, often handling complex and challenging projects.
ACHIEVEMENTS
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GMP Consultant
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Projects Completed
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Dossier Filling
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Vendor Audit
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Formulation Development
HOW IT WORK
Our Work Process
Designing and analysis
Project key features, structure, criteria for success and major deliverables are planned during the early phase of Project design. Designs are developed to meet the stakeholder’s requirement as well as the local and international regulatory requirements.
Creative solutions
Self-motivated and professional team having knowledge to identify any probable risks which may directly or indirectly impact on project. After identification we create a detailed plan with assessment of potential risk to ensure desire out put from project as intended.
Project monitoring & control
Establish the project baselines which includes scope of work, project schedule and tentative project budget. This helps seamless execution of all planned tasks.
Project launch
Prior to launch, an extensive planning carried out which includes project completion on time within budget, by ensuring sufficient resources in place for each critical aspect of project and work distribution to specified technical team members.