Quality Control (QC)™

Mode of Exam

• Online Exam:

  • Candidates can take the exam from any location using a secure online platform.

  • Proctored environment ensures exam integrity.

  • Multiple-choice questions (MCQs) with time limit.

• Offline / Center-Based Exam:

  • Conducted at GIPMC authorized centers across major cities.

  • Supervised by trained invigilators.

  • Same syllabus and format as online exam.

• Exam Format:

  • Computer-Based Test (CBT) or Paper-Based Test (PBT) depending on chosen mode.

  • Questions cover GMP, cGMP, WHO-GMP, GLP, ISO standards, analytical testing, and regulatory compliance.

  • Time limit: 60–90 minutes based on certification level.

• Flexibility:

  • Candidates can choose their preferred mode of exam while registering.

  • Online exams allow anywhere access, offline exams provide a structured center environment for hands-on support.

Duration of Exam

• Basic Level: 60 minutes

• Intermediate Level: 75 minutes

• Advanced Level: 90 minutes

Details:

• The exam duration varies based on the complexity and depth of the certification level.

• Includes multiple-choice questions (MCQs) covering GMP, cGMP, WHO-GMP, GLP, ISO standards, analytical testing, and regulatory compliance.

• Time is allocated to ensure candidates have sufficient opportunity to carefully read, analyze, and answer each question.

Tip for Candidates:

• Plan your time wisely; don’t spend too long on a single question.

• Use the initial minutes to review all questions and mark any for later review if needed.

Agar chaho, main iska combined Exam Pattern Table bhi bana du jisme:

• Level (Basic/Intermediate/Advanced)

• Duration

• Number of Questions

• Passing Marks

Closed Book Exam

• Nature of Exam:
  The Quality Control (QC)™ – Pharmaceutical Sector exam is a closed book examination, meaning candidates are not allowed to refer to textbooks, notes, or any external resources during the test.

• Purpose:

  • To assess true understanding of pharmaceutical quality control concepts.

  • Ensure candidates have practical knowledge of GMP, cGMP, WHO-GMP, GLP, ISO standards, and regulatory compliance.

  • Maintain the credibility and integrity of the certification.

• Exam Integrity:

  • For online exams, a secure proctoring system monitors the candidate.

  • For offline exams, invigilators supervise all candidates to prevent access to unauthorized materials.

• Candidate Preparation:

  • Focus on conceptual clarity and practical understanding rather than rote learning.

  • Utilize provided study materials, sample papers, and mock tests for preparation.

Retaking of Exam

• Eligibility for Retake:
  Candidates who do not pass the exam on their first attempt are eligible to retake the exam.

• Waiting Period:

  • A minimum waiting period of 15 days is required before scheduling a retake.

  • This allows candidates sufficient time to review study materials and prepare thoroughly.

• Number of Retakes:

  • Candidates may retake the exam up to 3 times within 6 months of initial registration.

  • Beyond this, candidates must re-register for the certification program.

• Retake Fee:

  • A nominal retake fee applies, typically 50% of the original exam fee (varies based on certification level).

• Preparation Tips for Retake:

  • Focus on weak areas identified in previous attempt.

  • Utilize mock tests and sample papers provided by GIPMC.

  • Review GMP, cGMP, WHO-GMP, GLP, ISO standards, and regulatory compliance thoroughly.

Certification Validity

• Lifetime Certification:
  The Quality Control (QC)™ – Pharmaceutical Sector certification awarded by GIPMC is valid for a lifetime. Once earned, professionals can showcase it throughout their career without expiry.

• Optional Continuing Education:

  • To stay updated with latest industry standards, regulatory changes, and best practices, candidates may opt for continuing education or refresher courses.

  • This helps maintain cutting-edge knowledge in GMP, cGMP, WHO-GMP, GLP, ISO standards, and regulatory compliance.

• Recognition:

  • The certificate is globally recognized by pharmaceutical organizations and regulatory bodies.

  • Professionals can leverage it for career advancement, job opportunities, and professional credibility.

• Digital Certificate:

  • Upon successful completion, candidates receive a digitally verifiable certificate.

  • Easy to share on LinkedIn, resumes, and company portals.

Trademark Acknowledgement

• Registered Trademark:
  Quality Control (QC)™ is a registered trademark of GIPMC (Global Institute of Professional Management Certification).

• Ownership:

  • All rights, titles, and interests in the QC™ certification program, logo, and associated materials are exclusively owned by GIPMC.

  • Unauthorized use of the trademark or certification name is strictly prohibited.

• Usage:

  • Candidates who successfully complete the QC™ certification are licensed to use the trademark in their resumes, LinkedIn profiles, business cards, and professional portfolios.

  • The trademark must always be used in conjunction with GIPMC certification, e.g., “Quality Control (QC)™ – Certified by GIPMC”.

• Legal Protection:

  • QC™ is protected under applicable intellectual property laws.

  • Any misuse, reproduction, or distribution without GIPMC authorization may lead to legal action.

Credits

• Course Development:
  Developed by industry experts, pharmaceutical quality assurance professionals, and GIPMC subject matter specialists.

• Content Contributors:

  • Experienced QA/QC Analysts from the pharmaceutical sector

  • Certified GMP, GLP, ISO trainers

  • Regulatory experts with hands-on knowledge of US FDA, EMA, MHRA, TGA guidelines

• Instructional Design:

  • Designed by GIPMC’s curriculum and e-learning specialists to ensure effective learning and practical application.

• Assessment & Certification:

  • Exam and evaluation prepared by GIPMC’s certified QA/QC team

  • Certification issued under the official GIPMC seal

• Special Thanks:

  • To all industry collaborators, advisory board members, and pharma professionals who contributed insights and best practices to ensure high-quality certification content.

Pre-Requisite

To enroll in the Quality Control (QC)™ – Pharmaceutical Sector certification, candidates should ideally meet the following prerequisites:

1. Educational Background:

   • Bachelor’s degree in Pharmacy, Life Sciences, Chemistry, Biotechnology, or related fields.

   • Graduates from other disciplines with interest in pharmaceutical quality control may also apply.

2. Work Experience (Optional but Recommended):

   • 1–2 years of experience in pharmaceutical manufacturing, QA/QC labs, or regulatory compliance is beneficial.

   • Helps in understanding GMP, cGMP, WHO-GMP, GLP, ISO standards, and regulatory frameworks practically.

3. Basic Knowledge:

   • Familiarity with laboratory procedures, analytical testing, and documentation practices is an advantage.

   • Ability to read and comprehend technical guidelines and SOPs.

4. Language Proficiency:

   • Exam and study materials are in English, so proficiency in reading and understanding English is required.

5. Technical Requirements (For Online Mode):

   • A computer/laptop with internet access for online learning and exam.

   • Basic skills in using web platforms and online assessments.

Note:

• There are no strict mandatory requirements; beginners with strong motivation can also enroll.

• Recommended to review provided study materials and mock tests before attempting the exam.