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Occupational Qualification · H6

Discretionary Grant · Upcoming

Health Products Code Compliance Officer

QCTO Aligned Audit-ReadyCHIETA
NQF Level
NQF Level 5
Credits
34
Duration
—
SAQA ID
125104
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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

Curriculum Alignment MatrixCRN ZA-SDP-2026-089
Curriculum Alignment Matrix — page 1
Curriculum Alignment Matrix — page 2
Curriculum Alignment Matrix — page 3
Curriculum Alignment Matrix — page 4
Curriculum Alignment Matrix — page 5
Page 1 of 5

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 credits

Theory, 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

Sub-total credits19
QCTO & CHIETA AlignedSAQA 125104

Qualification 125104 · Curriculum Architecture

Occupational Certificate: Health Products Code Compliance Officer · NQF Level 5 (34 Credits)

Filter View
§ 01

Three Curriculum Pillars

19
Credits

Knowledge Modules

Classroom & E-Learning

KM-01 to KM-04 · 4 modules
  • Facilitated lectures & self-study
  • Written question banks
  • Formative comprehension checks
9
Credits

Practical Skill Modules

Simulated Line Tasks

PM-01 to PM-02 · 2 modules
  • Simulated line tasks
  • Observation rubrics
  • Structured task sheets
6
Credits

Work Experience Modules

On-the-Job Production

WM-01 to WM-01 · 1 modules
  • On-the-job rotation
  • Mentor logbooks
  • Workplace sign-offs
§ 02

Evidence & Audit Pipeline

Learner Portfolio of Evidence (PoE)
Owner · Candidate
▾
1
Admin & Registration

ID, learner contract, induction pack, POPIA consent.

2
Knowledge Evidence

Written assessments & question banks — KM-01 to KM-07.

3
Practical Evidence

Task sheets, observation rubrics, assessor photos.

4
Workplace Evidence

Logbooks, mentor sign-offs, supervisor letters.

Assessor Master File
Owner · Registered Assessor
▾
5
Assessment Reports

Judgements, learner feedback, remediation agreements, appeals log.

Internal Moderation & Quality File
Owner · Moderator / SDP
▾
6
Moderation Evidence

10% sampling matrix, HACCP/LOTO compliance sheets, SDP sign-off.

§ 03

Final Accreditation Gateway

Step 1
Statement of Results

Issued by the accredited Skills Development Provider once internal moderation is signed off.

Step 2
EISA Readiness Declaration

Provider submits declaration + PoE to the Assessment Quality Partner (AQP).

Step 3
National Qualification Certificate

QCTO awards the SAQA-registered certificate on successful EISA outcome.

Learner Certified · Uploaded to National Learner Records Database (NLRD)

Audit & Compliance

Evidence & Audit Pipeline

From portfolio assembly to external sign-off — the exact route your evidence travels.

  1. Step 1

    PoE Assembly

    Learner evidence, formative records and logbook entries filed against the alignment matrix.

  2. Step 2

    Internal Assessment

    Registered assessor judges each KM/PM/WM outcome using the supplied instruments.

  3. Step 3

    Internal Moderation

    Sampling and verification of assessor decisions, with remediation loop before submission.

  4. 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

View on SAQA

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
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Most selected

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
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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
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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.

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Moderation Consultation

External moderation dry-run on your PoE + delivery pack. Written report with fixes before your real audit. From R4,900.

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The 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.