Our Services
GAP Analysis
GAP Analysis is a process that compares actual performance or results with expected or desired. The method provides a way to identify strategies, structures, capabilities, processes, practices, technologies, or non-optimal or missing skills, and then recommends steps that will help the company achieve its goals.
View More..Audits
CostaricaPharma follows Auditing Practise to ensure the constant quality of pharmaceutical products and industry standards.Following are the consideration we follow while performing GMP Auditing
View More..Validation
CostaricaPharma will help to evaluate the suitability of products, equipment, and machinery. Costarica provides expert and objective assessments that help ensure that strengths are recognized and weaknesses are addressed.
View More..Risk Management
Risk management should be seen as a constant Quality Management process.Risk Management activities include processes, procedures to maintain and verify that risk measures are taken and are effective.We help in identifying the Risks and offers Risk Management Programs to eradicate the Risk. Our Risk Management Program
View More..Regulatory Support
Wehavea proven history of effective communication with various regulatory authorities in India. As a regulatory consultant, we ensure that communications received from regulatory authorities are interpreted and understood correctly to ensure that the issues raised are adequately addressed without unnecessary waste of time and resources.
View More..Vendor Qualification
Vendor Qualification is a combination of Activities required to ensure that a vendor will meet the professional and regulatory expectation of the sponsor
View More..Training
We specialize in offering training on different concepts of Pharmaceutical related programs like Quality Control, Quality Assurance, GMP, Regulatory, Validation, etc across Globally and Nationally. Our Core Team of Trainers is expertise in offering Industrial-level Training to the organization’s staff and core members.
View More..DMF / DOSSIER
Our Service includes Developing Regulatory Strategies, Comprehensive Documentation, Submission and Archiving of Documents. Regulatory Department also oversees the compliance program, ensuring that all practices conform to the constantly changing regulatory requirements.
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