Occupational Qualification · H6
Discretionary Grant · UpcomingHealth Products Code Compliance Officer
- NQF Level
- NQF Level 5
- Credits
- 34
- Duration
- —
- SAQA ID
- 125104
Official QCTO Registry Profile
Source: SAQA / QCTO registry- SAQA ID
- 125104
- Min Credits
- 34
- Registered
- 2025-11-13
- Re-registration
- 2029-11-13
- Field
- Field 09 - Health Sciences and Social Services
- Sub-field
- Curative Health
Sample Asset Preview





Overview & Scope
Programme Profile
- Target Designation
- Certified Health Products Code Compliance Officer Practitioner
- Competency Focus
- Master specialised practical applications, safety criteria, and regulatory mandates required of a qualified Health Products Code Compliance Officer.
- Academic Weight
- Full national recognition at NQF Level 5 yielding 34 credits upon successful PoE verification.
- Work Opportunities
- Deployment across As a qualified health products code compliance officer, you can find employment opportunities in Chemical, Plastics, Glass, Mining including hospitals, clinics, home care agencies, NGOs, and community health centres. Your skills will be in demand across both public and private sectors, and you may also choose to work as an independent contractor or start your own business in this field. operations under CHIETA scope.
- Audit Objective
- Bridges operational skills deficits under the governing CHIETA quality matrix.
- Value Proposition
- Measurable, legally compliant skills that optimise productivity, satisfy Workplace Skills Plans (WSP), and unlock B-BBEE scorecard weight.
Introduction▾
Designed as a Occupational Certificate at NQF Level 5 worth 34 credits, the Health Products Code Compliance Officer equips you with both theoretical understanding and hands-on capabilities. You will learn to perform complex tasks, solve real-world problems, and adapt to the demands of a dynamic work environment. This qualification is your stepping stone to becoming a confident, capable professional.
Purpose▾
The purpose of Occupational Certificate: Health Products Code Compliance Officer is to prepare a learner to operate as a Health Product Code Compliance Officer. A Health Product Code Compliance Officer conducts compliance activities in a health product regulatory environment. They ensure compliance of promotional and educational material and activities to applicable industry code regulations. A qualified learner will be able to: • Conduct/perform code compliance activities on health products. Achieving this part-qualification will provide several benefits to the learner, including: • Being able to carry out a range code compliance activities with respect to promotional material and activities related to health products. • Acquiring in-depth knowledge of code compliance activities and processes for health products • Taking an important step into the health products sector with the prospect of acquiring higher or related qualifications in the field. • Acquisition of a formal qualification in health products environment if they do not already have a qualification • Increasing the opportunity of gaining employment with companies that manage health product applications for registration and licensing. Considering South Africa's huge unemployment rate, a qualification like this has the potential to get learners into meaningful employment. Typical graduate attributes include proficiency, efficiency, and effectiveness in preparing dossiers for registration and renewal of health products. The Health Products Code Compliance Officer (HPCCO) is a person of integrity and high ethical standards as they ensure that all promotional material and activities designed for health products meet the requirements of the regulatory framework.
Entry Requirements▾
Recognition of Prior Learning (RPL): RPL for Access to Training: Learners may use the RPL process to gain access to training opportunities for a part-qualification if they do not meet the formal, minimum entry requirements for admission. RPL assessment provides an alternative access route into a part-qualification. Such an RPL assessment may be developed, moderated and conducted by the accredited Skills Development Provider which offers that specific part qualification. Such an assessment must ensure that the learner is able to display the equivalent level of competencies required for access, based on the NQF level descriptors. RPL for Access to the External Integrated Summative Assessment (EISA): For exemption from modules through RPL, learners who have gained the stipulated competencies of the modules of a part-qualification through any means of formal, informal or non-formal learning and/or work experience, may be awarded credits towards relevant modules, and gaps identified for training, which is then concluded. Entry Requirements: An NQF Level 4 qualification, with Mathematics and Science.
SAQA Rationale▾
No health product may be sold in South Africa unless it has been registered with an appropriate regulatory body. This qualification covers medicines, medical devices and in vitro devices (IVDs), complementary medicines, personal care products and veterinary products. Currently, the South African Health Products Authority (SAHPRA) registers health products as defined by the Medicines Act 101 of 1965 and its Amendments - whether they are manufactured local or abroad - to ensure safety, efficacy, and quality The marketing or promotion of health products is very strictly controlled through application of the relevant sector codes by the Health Products Code Compliance Officer (HPCCO) or a Responsible Pharmacist (RP) or an Authorised Representative (AR) as long as they are trained as a HPCCO. The qualification plays a very critical role in ensuring that sector codes are applied to all promotional and educational materials and activities. Unfair promotional practices carried out impact negatively on other companies promoting their products through fair practices. In spite of their critical role, there is no qualification registered on the NQF for this much-needed part-qualification. This is the first time a qualification for this occupation is being developed. Current training is disparate and carried out by companies that register, license and market health products. There is a need to standardise such disparate training and set the benchmark for the occupation. As the number of health products grows significantly in view of scientific advancement (the plethora of health products being a case in point), this qualification becomes critical to ensure that the public is exposed to promotional material for health products that has been subject to regulatory scrutiny prior to approval. The challenges stemming from misinformation regarding health products will always be there and this emphasises the responsibility of the Health Products Code Compliance Officer (HPCCO). The safety of the public is paramount when it comes to using or consuming health products and the application of the relevant compliance codes will strengthen the public's confidence in products that have been approved. Additionally, ensuring that promotional activities for health products occur within the ambit of the regulatory framework maintains fairness in the sector and companies abiding by the compliance codes are not affected negatively. Hence, this part-qualification ensures that the interests of the health product sector are protected. The part-qualification has the potential of creating employment as it is needed in the industry and there is a potential uptake of the qualification by significant number of learners. Increased employment will translate into increased benefits for the economy. Typical learners will be those currently practising as Health Products Code Compliance Officers who have been operating without training on a formal qualification. Other learners could include matriculants or those with a relevant higher education qualification wishing to enter the health products regulatory field. Learners working towards this part-qualification will find that the acquisition of competencies embedded in the modules will either enable them to either obtain employment or add value to their job performance if they are already employed. In the development of this qualification, the following stakeholders were consulted: • Training providers. • Regulator. • Employers/employer organisations. There are no similar Qualification(s) and Part-Qualifications registered on the NQF, and no Skills Programmes approved by the QCTO.
Learning Assumed to be in Place & RPL▾
Recognition of Prior Learning (RPL): RPL for Access to Training: Learners may use the RPL process to gain access to training opportunities for a part-qualification if they do not meet the formal, minimum entry requirements for admission. RPL assessment provides an alternative access route into a part-qualification. Such an RPL assessment may be developed, moderated and conducted by the accredited Skills Development Provider which offers that specific part qualification. Such an assessment must ensure that the learner is able to display the equivalent level of competencies required for access, based on the NQF level descriptors. RPL for Access to the External Integrated Summative Assessment (EISA): For exemption from modules through RPL, learners who have gained the stipulated competencies of the modules of a part-qualification through any means of formal, informal or non-formal learning and/or work experience, may be awarded credits towards relevant modules, and gaps identified for training, which is then concluded. Entry Requirements: An NQF Level 4 qualification, with Mathematics and Science.
Exit Level Outcomes▾
1. Interpret and apply appropriate procedures and criteria to conduct/perform code compliance activities on health products.
Learning Material Included
- Learner Guide (Theory and Knowledge Modules)
- Facilitator Guide
- Workplace Logbook
- Formative and Summative Assessment
- Assessor Guide & Marking Memorandum
- SETA / QCTO Alignment Matrix
- Administrative & Onboarding Pack
- Implementation Plan
Moderator-Ready Curriculum Breakdown
7 modules · 34 creditsTheory, regulatory and safety knowledge. Each row carries the registered module code, NQF level and credit weight used for formative assessment rubric mapping.
- 242213-001-00-KM-015 cr
Overview of Current Health Products Industry/Sector
NQF Level 5
- 242213-001-00-KM-038 cr
Health Products
NQF Level 5
- 242202-001-00-KM-053 cr
Codes of Practice for HPRAs
NQF Level 5
- 242213-001-00-KM-083 cr
Professional Conduct
NQF Level 4
Qualification 125104 · Curriculum Architecture
Occupational Certificate: Health Products Code Compliance Officer · NQF Level 5 (34 Credits)
Three Curriculum Pillars
Knowledge Modules
Classroom & E-Learning
- Facilitated lectures & self-study
- Written question banks
- Formative comprehension checks
Practical Skill Modules
Simulated Line Tasks
- Simulated line tasks
- Observation rubrics
- Structured task sheets
Work Experience Modules
On-the-Job Production
- On-the-job rotation
- Mentor logbooks
- Workplace sign-offs
Evidence & Audit Pipeline
Learner Portfolio of Evidence (PoE)Owner · Candidate▾
Admin & Registration
ID, learner contract, induction pack, POPIA consent.
Knowledge Evidence
Written assessments & question banks — KM-01 to KM-07.
Practical Evidence
Task sheets, observation rubrics, assessor photos.
Workplace Evidence
Logbooks, mentor sign-offs, supervisor letters.
Assessor Master FileOwner · Registered Assessor▾
Assessment Reports
Judgements, learner feedback, remediation agreements, appeals log.
Internal Moderation & Quality FileOwner · Moderator / SDP▾
Moderation Evidence
10% sampling matrix, HACCP/LOTO compliance sheets, SDP sign-off.
Final Accreditation Gateway
Issued by the accredited Skills Development Provider once internal moderation is signed off.
Provider submits declaration + PoE to the Assessment Quality Partner (AQP).
QCTO awards the SAQA-registered certificate on successful EISA outcome.
Audit & Compliance
Evidence & Audit Pipeline
From portfolio assembly to external sign-off — the exact route your evidence travels.
- Step 1
PoE Assembly
Learner evidence, formative records and logbook entries filed against the alignment matrix.
- Step 2
Internal Assessment
Registered assessor judges each KM/PM/WM outcome using the supplied instruments.
- Step 3
Internal Moderation
Sampling and verification of assessor decisions, with remediation loop before submission.
- Step 4
External Moderation
SETA/QCTO desktop audit and certification upload against registered credits.
Broken Standard vs i2Graduates Standard
The measurable delta between improvised material and an audit-ready suite.
Broken Standard
i2Graduates Standard
Curriculum Mapping
Photocopied guides with mismatched outcomes
4 KM + 2 PM + 1 WM modules mapped to NQF Level 5
Assessment Bank
Missing formative and summative assessments
Pre-validated assessment bank per module
Alignment Evidence
No alignment matrix — audit fails
CHIETA alignment matrix included
Facilitation
Facilitators improvise Health Products Code Compliance Officer delivery
Facilitator scripts + learner activities per credit
Portfolio of Evidence
PoE gaps flagged in moderation
PoE templates that survive external moderation
Pricing & Delivery Tiers
Base licence from R56 700
Digital Master Suite
Editable master files, licensed to your SDP
- Learner Guide, Facilitator Guide & Assessment Suite
- Workplace logbook + alignment matrix (editable)
- Instant digital delivery under institutional licence
- Free minor corrections for 12 months
Turnkey Print & Bound Package
Printed, bound and couriered per learner
- Everything in the Digital Master Suite
- Full-colour print, wire-bound learner packs
- Per-learner PoE folders and dividers
- Nationwide courier with tracked delivery
Full Enterprise Accreditation Bundle
Assets plus accreditation support end-to-end
- Everything in the Print & Bound Package
- Bespoke QMS build mapped to your scope
- Moderation dry-run + written remediation report
- Brand & metadata integration across the suite
Complementary Services
Optional add-ons that harden your accreditation scope before an external audit.
Bespoke QMS Build
We author your Quality Management System — policies, procedures, records, matrices — mapped to your accreditation scope. From R18,500.
Request QuoteModeration Consultation
External moderation dry-run on your PoE + delivery pack. Written report with fixes before your real audit. From R4,900.
Book Moderation SessionThe i2Graduates Quality Guarantee
Every page of this bundle is checked for sequence and structural accuracy — no missing pages, no shortcuts. You get pre-validated assessment instruments ready to survive rigorous compliance moderation, wrapped in a curriculum your facilitators will enjoy teaching.
