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Pharmacists Registration (Practising Certificates) Regulations 2008

Overview of the Pharmacists Registration (Practising Certificates) Regulations 2008, Singapore sl.

Statute Details

  • Title: Pharmacists Registration (Practising Certificates) Regulations 2008
  • Act Code: PRA2007-S438-2008
  • Legislation Type: Subsidiary legislation (SL)
  • Authorising Act: Pharmacists Registration Act 2007 (Act 48 of 2007)
  • Enacting Authority: Singapore Pharmacy Council (with Minister for Health approval)
  • Citation: Pharmacists Registration (Practising Certificates) Regulations 2008
  • Commencement: 1 September 2008
  • Current Version (as provided): Current version as at 27 Mar 2026
  • Key Provisions: Regs 2 (definitions), 3 (application), 4 (application form/fees), 5 (late fees), 5A (certified true copy), 5B (duplicate), 6 (CPE-based grant/renewal), 7 (CPE programme list), 8 (fees), 9 (duration), 10 (transitional)
  • Schedules: First Schedule (fees); Second Schedule (CPE requirements)

What Is This Legislation About?

The Pharmacists Registration (Practising Certificates) Regulations 2008 (“Practising Certificates Regulations”) set the administrative and regulatory framework for how registered pharmacists obtain and renew practising certificates in Singapore. In practical terms, the Regulations operationalise the Pharmacists Registration Act 2007 by specifying the conditions, processes, and fees that govern whether the Singapore Pharmacy Council (“Council”) will grant or renew a pharmacist’s practising certificate.

The central policy objective is professional regulation through continuing professional education (“CPE”). The Regulations require pharmacists to meet specified CPE point thresholds within defined qualifying periods, and they empower the Council to refuse grant or renewal if those requirements are not satisfied. The Regulations also address operational issues that commonly arise in practice: late applications, requests for certified true copies, duplicates of lost or damaged certificates, and the validity period of practising certificates.

Although the Regulations are technical, they have direct consequences for practising pharmacists and for pharmacists who are not in active practice. The Regulations distinguish between pharmacists who are actively practising and those who are not, and they impose additional procedural steps and conditions for non-active pharmacists seeking to rely on certain CPE items or to resume active practice.

What Are the Key Provisions?

1. Definitions and core concepts (Regulation 2)
The Regulations define key terms that drive the CPE system and eligibility. Notably, “active practice” includes pharmacy practice on a full-time or part-time basis, or as a locum. This definition matters because Regulation 6 treats active and non-active pharmacists differently for renewal purposes and for resumption of active practice.

Regulation 2 also defines “continuing professional education point” as a point obtained by successfully completing an activity, course or programme that is in the list made under Regulation 7. This ties the CPE obligation to an official Council-maintained list, which is important for compliance: pharmacists must ensure that their learning activities are properly recognised and mapped to the correct point allocations.

2. Scope of application (Regulation 3)
Regulation 3 provides that the Regulations apply to any person who is registered or deemed to be registered as a pharmacist under sections 16 or 17 of the Pharmacists Registration Act 2007. However, Regulation 6 (the CPE-based refusal power) does not apply to a person making a first-time application for the grant or renewal of a practising certificate under these Regulations. This means that the CPE refusal mechanism is not automatically applied to initial entrants in their first practising certificate application cycle.

3. Application mechanics and late fees (Regulations 4 and 5)
Under Regulation 4, an application for grant or renewal of a practising certificate under section 23 of the Act must be made in the form published on the Council’s website and must be accompanied by the applicable fees in the First Schedule. This is a procedural requirement: failure to use the correct form or to include the correct fee can create administrative non-compliance even if the pharmacist has otherwise met substantive requirements.

Regulation 5 introduces an additional fee regime for late applications. If an application is made less than one month before expiry, or after expiry, the “appropriate fee for late application” must be paid in addition to the application fee. For practitioners, this is a compliance lever: timely renewal submissions can avoid extra costs and reduce the risk of practising without a valid certificate.

4. Certified true copies and duplicates (Regulations 5A and 5B)
Regulation 5A (inserted by amendment effective 4 September 2012) allows a pharmacist to apply for a certified true copy of a practising certificate. The application must be made in the form and manner required by the Council and must be accompanied by the appropriate fee in the First Schedule.

Regulation 5B is more detailed and addresses duplicates. If a practising certificate is lost, destroyed, defaced, or obliterated such that particulars are illegible, the holder must “immediately” apply for a duplicate. The Council must issue a duplicate if satisfied of the circumstances and upon payment of the appropriate fee, but the issuance is subject to conditions:

  • Defaced/obliterated certificates: no duplicate unless the original is returned to the Council.
  • Lost/destroyed certificates: no duplicate unless the holder makes a statutory declaration of loss or destruction and furnishes it to the Council.
  • Effect: a duplicate has the same effect as the original.
  • Found original after duplicate: if the original is later found, the holder must return the duplicate for cancellation within 14 days.

Regulation 5B(7) creates an offence for failure to comply with the return-for-cancellation requirement, with liability on conviction to a fine not exceeding $1,000. This is a practitioner-relevant provision because it creates a clear post-duplicate compliance obligation and a potential criminal exposure for non-return.

5. CPE-based grant/renewal and non-active practice rules (Regulation 6)
Regulation 6 is the regulatory core. It provides that the Council may refuse to grant or renew a practising certificate unless the applicant satisfies the Council that they have fulfilled the requisite CPE requirements indicated against the relevant description of the applicant in the first column of the Second Schedule.

Compliance is measured in two ways:

  • Point accumulation: the applicant must accumulate not less than the requisite CPE points within the qualifying period set out in the Second Schedule.
  • Category mix: a specified percentage of the requisite points must come from specified types or categories of programmes, if the Second Schedule so provides.

Regulation 6(2) addresses pharmacists who are not in active practice. Such pharmacists cannot rely on “item 9” of the Second Schedule for renewal unless they (a) file a declaration in the relevant form available on the Council’s website and (b) obtain the Council’s approval to rely on that item. This is a procedural gatekeeping mechanism: even if a non-active pharmacist has some CPE, they may be barred from using a particular CPE item unless the Council approves.

Regulation 6(3) further addresses resumption of active practice. A non-active pharmacist who has satisfied Regulation 6(2) may resume active practice only if, in the 12 months immediately preceding the date they indicated to the Council that they wish to resume active practice, they obtain at least 25 CPE points, with at least 30% from pharmaceutical care programmes. This creates a “re-entry” training threshold and a minimum content mix, which is significant for risk management and patient safety.

Regulation 6(4) provides a discretionary safety valve: the Council may grant or renew even if the applicant cannot satisfy the requisite CPE requirements in “special circumstances” as it determines. Under Regulation 6(5), the Council may impose reasonable conditions in exercising this discretion. Practitioners should treat this as an avenue for relief, but one that is fact-sensitive and subject to Council discretion.

6. CPE programme designation (Regulation 7)
Regulation 7 requires the Council to designate and maintain a list of activities, courses and programmes with corresponding CPE points. The Council may categorise items and designate specific items for various classes or descriptions of pharmacists. This provision is crucial for compliance planning: pharmacists should confirm that their planned activities are on the Council’s list and that they fall within the correct category for the required point mix.

7. Fees, exemptions, and remissions (Regulation 8)
Regulation 8(1) makes the First Schedule fees payable to the Council. Regulation 8(2) empowers the Council, subject to conditions it directs, to exempt persons or classes from all or any fees. Regulation 8(3) similarly empowers the Council to remit or refund fees in whole or in part in particular cases or classes. For practitioners, this is relevant when advising clients on hardship, administrative errors, or special circumstances where fee relief may be sought.

8. Duration of practising certificate (Regulation 9)
Regulation 9 provides that a practising certificate is valid for two years or such shorter period as specified in the certificate. This affects renewal planning and the timing of CPE accumulation within qualifying periods.

9. Transitional provision (Regulation 10)
Regulation 10 contains a transitional mechanism for pharmacists who obtained CPE points between 1 September 2006 and 31 August 2008 under a prior scheme established by the Singapore Pharmacy Board. The extract provided is truncated, but the structure indicates that certain previously earned points may be recognised for transitional purposes. Transitional provisions often matter for pharmacists whose CPE history spans the regulatory change; practitioners should verify the full text in the official legislation database to determine the exact recognition and calculations.

How Is This Legislation Structured?

The Regulations are structured as follows:

  • Part/Section framework: The Regulations are organised into numbered regulations (1 to 10) plus two schedules.
  • Regulation 1: Citation and commencement (1 September 2008).
  • Regulation 2: Definitions of key terms such as “active practice” and “continuing professional education point”.
  • Regulation 3: Application of the Regulations to registered/deemed registered pharmacists, with a carve-out for first-time applications regarding Regulation 6.
  • Regulations 4–5B: Application procedures, late fees, certified true copies, and duplicates (including statutory declaration and return/cancellation obligations).
  • Regulations 6–7: CPE-based grant/renewal requirements and the Council’s designation of CPE programmes and points.
  • Regulations 8–9: Fees and duration of practising certificates.
  • Regulation 10: Transitional provision recognising CPE points earned under an earlier scheme.
  • First Schedule: Fees.
  • Second Schedule: CPE requirements, including qualifying periods and point/category rules for different pharmacist descriptions.

Who Does This Legislation Apply To?

The Regulations apply to persons who are registered or deemed to be registered as pharmacists under the Pharmacists Registration Act 2007. In practice, this includes pharmacists seeking to obtain or renew a practising certificate under section 23 of the Act.

All such pharmacists are subject to the procedural requirements for applications and fees, and—except for first-time applications—are subject to the Council’s power to refuse grant or renewal based on CPE compliance under Regulation 6. The Regulations also specifically address pharmacists who are not in active practice, imposing additional declaration/approval steps and re-entry CPE thresholds if they wish to resume active practice.

Why Is This Legislation Important?

For practitioners, the Regulations are important because they directly determine whether a pharmacist can lawfully practise under a valid practising certificate. The CPE framework is not merely advisory: it is embedded in the Council’s discretion to refuse grant or renewal. This makes CPE compliance a licensing risk area, requiring careful tracking of points, qualifying periods, and programme categories.

The Regulations also have practical administrative consequences. Late applications trigger additional fees, and lost or damaged certificates require formal processes (including statutory declarations and return obligations). These provisions can become contentious in disputes about whether a pharmacist complied with administrative requirements and whether the Council properly exercised its discretion.

Finally, the “special circumstances” discretion in Regulation 6(4) and the Council’s ability to impose reasonable conditions provide a structured pathway for relief. However, because the discretion is Council-determined, legal practitioners should prepare evidence and submissions addressing both substantive CPE shortfalls and the reasonableness of any proposed conditions.

  • Pharmacists Registration Act 2007 (Act 48 of 2007) — authorising framework for practising certificates and the Council’s regulatory powers

Source Documents

This article provides an overview of the Pharmacists Registration (Practising Certificates) Regulations 2008 for legal research and educational purposes. It does not constitute legal advice. Readers should consult the official text for authoritative provisions.

Written by Sushant Shukla

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