About Ally

Ally Compounding Pharma is registered with the Pharmacy Board of Malaysia and has full time pharmacist(s) licensed to offer compounded medications in accordance with Poisons Act 1952 and Good Compounding Practice​
Any request for compounded medications must have a valid prescription written by a registered medical practitioner, dentist or veterinary officer as stipulated in Section 21 of Poisons Act 1952.
Compounded medications can only be prescribed and prepared when
a) A registered product is unavailable
b) A registered product with similar therapeutic effect is unavailable
c) A registered product is unsuitable
d) When undertaking research sanctioned by a recognized human research ethics committee 

Our Responsibility

Ally Compounding Pharma is responsible for ensuring all medications are safely compounded based on best practice and guidelines. Prescribers are responsible for ensuring the correct treatment and dose for their patients.​

Return Policy

All sales are final. There will be no exchange, replacement or refund on compounded medications EXCEPT where item is damaged or wrongly delivered.  In this case, please notify us within 7 working days from the invoice date.

Our Quality

At Ally Compounding Pharma, we advocate quality and safety in compounding to ensure patients receive the best possible pharmaceutical care. Our commitment towards this is reflected in every aspect of pharmaceutical compounding.

​Professionally Trained

  • Our pharmacist is trained by Medisca, a leading FDA-registered supplier of quality pharmacy compounding products.
  • Our pharmacist is deeply involved in every step of the compounding process; from reviewing the prescription to calculating formula, weighing, compounding, validating, labelling, packaging and final dispensing.
  • Our pharmacist conducts in-house training for all pharmacy technicians

​​Raw Material Selection

  • Our materials are sourced from reputable FDA registered suppliers and GMP certified manufacturers; and meet the quality stated in the USP, BP, PhEur, JP, NF or equivalent.
  • Certificates of analysis are available for all materials.
  • We implement rigorous high-quality compounding preparatory techniques (e.g. proper trituration, geometric addition, levigation, calibration) and procedures (e.g. SOPs, verifications, master formulation record)

Equipment and Facilities

  • Strict controlled environment in the laboratory ensures quality and purity of raw materials are preserved.
  • Compounding activities are conducted in designated areas inside a biological safety cabinet equipped with HEPA filter and UV light for sterilisation.
  • Our capsuling device is patented, CE certified and is able to achieve capsule fill weights ± 1-2% of average.
  • We use a cutting edge planetary mixer to compound transdermal preparations that are homogeneous, deaerated and with low risk of contamination.
  • Our equipment and devices have Certificate of Compliance and undergo routine preventive maintenance.

Quality Control

Compounding Resources
To ensure accuracy and completeness, all compounded medications are subjected to qualitative and quantitative physical testing as per USP <795> and <1163>
We subscribe to several compounding resources which allow us to access formula database, consultation with compounding experts, guidelines, best practices, journals, peer-reviewed studies etc.

Pharmaceutical Waste Management

Safety of the general public is just as important and is something that we are committed to. We engage qualified waste management company to safely dispose of our pharmaceutical waste, in particular hormones.