About the pharmacy
ReliantRx is a sterile compounding pharmacy in the Philippines. Every preparation is compounded against a valid prescription for a named patient, under a PRC-licensed supervising pharmacist.
This page carries the licence record, the USP chapters followed, and the release procedure. Where a number is not yet published here, it reads [TBD] rather than being paraphrased.
Four credentials a prescriber can verify with the issuing body, without asking us first.
FDA License to Operate
[TBD]
Number and expiry date. Issued by the Philippine FDA and verifiable in its public register.
Supervising pharmacist
PRC [TBD]
Licence number of the pharmacist supervising every preparation. Checkable against the PRC roster.
Cleanroom classification
ISO [TBD]
Classification, certifying body, and date of last certification. Certificates on file at the pharmacy.
Controlled substances
None
No controlled substances are dispensed, so PDEA registration does not apply to this facility.
Registered business name
[TBD]
Facility address
[TBD]
Year the pharmacy began operating
[TBD]
Professional affiliations
[TBD]
USP standards
A chapter number tells a prescriber exactly which practice a preparation was made under. Each chapter below is listed with its status at this facility; unconfirmed status reads [TBD].
<797>
Sterile preparations — followed. Scope of compliance [TBD]
<795>
Non-sterile preparations — whether offered at all [TBD]
<800>
Hazardous drugs — applicability to this facility [TBD]
Records
Compounding records are retained per preparation. Retention period [TBD]
The facility
Preparation takes place in a facility equipped for sterile work: controlled air, defined garbing and technique, and environmental monitoring on a fixed schedule. Certificates and monitoring records are held at the pharmacy.
Primary engineering control
[TBD]
Environmental monitoring interval
[TBD]
Certification body and last date
[TBD]
Quality practice
Nothing is prepared for stock. Each preparation is checked against the written order — patient, drug, strength, vehicle, dosage form — and released by the supervising pharmacist.
Capabilities & dosage forms →01
Components are received against supplier documentation and logged to the preparation record. Supplier qualification [TBD]
02
Calculations and measurements are independently checked before compounding proceeds.
03
The pharmacist releases against the written order and signs the record. Labelling includes beyond-use date.
04
Cold chain is held from release to handover. Packaging method and monitoring [TBD]
Why there are no bios here
What decides whether a preparation is safe is the licence, the chapter, the technique, and the release check — not a career summary. So this page publishes the record and leaves the profiles out.
Prescribers who want to speak with the supervising pharmacist directly can arrange it through the pharmacy.
Certificates, monitoring records, and licence copies are provided to prescribers on request. Do not send patient information by email or form.