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Este documento invita a los mayoristas de productos farmacéuticos veterinarios a presentar solicitudes para la precalificación, que formará parte de la adquisición de productos y equipos veterinarios
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How to fill out prequalification of pharmaceutical suppliers

01
Gather essential documentation such as company profile, product catalog, and quality assurance certificates.
02
Review the prequalification guidelines provided by the regulatory authority or organization.
03
Complete the prequalification application form accurately, ensuring all fields are filled.
04
Provide detailed information on manufacturing processes and facilities.
05
Submit evidence of prior quality assessments or inspections by relevant authorities.
06
Include samples of product labeling and packaging.
07
Ensure compliance with international quality standards, such as WHO or GMP.
08
Submit the application along with all necessary documents to the designated regulatory body.

Who needs prequalification of pharmaceutical suppliers?

01
Pharmaceutical manufacturers seeking to supply products to healthcare facilities or government health programs.
02
Regulatory authorities assessing potential suppliers before approving contracts.
03
Organizations involved in procurement of pharmaceuticals to ensure product quality and safety.
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Prequalification of pharmaceutical suppliers is a process that assesses the capability and reliability of suppliers to provide quality pharmaceutical products that meet regulatory standards. It ensures that suppliers comply with predefined quality assurance criteria.
Pharmaceutical manufacturers and suppliers seeking to offer their products to governmental and institutional buyers, as well as those wanting to meet international standards, are required to file for prequalification.
To fill out the prequalification of pharmaceutical suppliers, applicants must gather necessary documentation, including company information, product specifications, quality control systems, and compliance records. They then fill out the prequalification application forms as per the regulatory guidelines and submit them for review.
The purpose of prequalification is to ensure that suppliers provide safe, effective, and quality pharmaceutical products. It helps mitigate risks associated with substandard products and promotes confidence among buyers and regulatory bodies.
Information that must be reported includes supplier details, quality assurance systems, product information, compliance with regulatory standards, manufacturing practices, past performance records, and any relevant certifications or licenses.
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