April 2011

SANA Pharma has succeeded in development and scaling up paracetamol injection dossier.
It's well known that formulation and processing of paracetamol injection is very crucial in obtaining stable product physically (e.g. no color change) and chemically (e.g. no drop in assay and no rise in degradation on product).
The product which has been manufactured according to SANA Pharma dossier has shown excellent stability profile.

July 2010

SANA Pharma has been contracted to qualify the JFDA Laboratory (Drug Quality Control Laboratory) according to ISO/IEC 17025 requirements.
This contract is sponsored by EU-Jordanian Partnership and will take about 18 months for implementation.
SANA Pharma is the first Jordanian expertise firm that won an EU-Sponsored contract.
Through this contract, the JFDA Laboratory will be qualified to be one of the few accredited national laboratories within Middle Eastern Region.
SANA has been entrusted for this project after a highly competetive selection proccess in recognition for its technical and expertise competencies.

June 2010

SANA Pharma has signed Pharmaceuticals development contract with a leading Swiss pharmaceutical manufacturing company. This contract is covering development of OTC Pharmaceuticals and preparing their CTD files to be registered and manufactured within EU countries.

June 2010

The microlab of Sana Pharma has been inspected and accredited by JFDA . Accordingly , Sana Pharma has signed contract analysis agreement with a local Pharmaceutical company as well as different cosmotics companies to conduct various microbial testing.

Nov. 2009

SANA Pharma Laboratories has been accredited by Jordan Accreditation System (JAS) according to ISO/EC 17025 to carry out all physical and chemical tests of pharmaceuticals, cosmetics, and food products. This project has been implemented at SANA laboratories as part of its policy to improve quality of analytical service provided as third party reference laboratories.
SANA Pharma by this accreditation is the first pharmaceutical reference laboratory in the region that is applying and has been accredited according to ISO 17025 regulations.

Oct. 2009

SANA Pharma has participated in the round 29 & round 30 intra laboratory proficiency testing program that has been conducted by LGC Standard (a UKAS accredited international provider of proficiency testing (PT) systems).
The SANA Pharma results ranked the 3rd amongst 34 international pharmaceutical labs with respect to results closeness to the assigned values (z-score).

Aug. 2009

SANA Pharma has successfully conducted training workshop on "HPLC method development based on the molecular structure of pharmaceuticals" . 40 analyst participated in this workshop from Jordan pharmaceutical industry, JFDA lab and other Arab companies. The course was introduced as an interactive discussion for case studies covering real models. This course is the second one held by SANA pharma among group of courses targeting specific technical subjects after assessment of training needs.
Next course: how to increase sensitivity and selectivity in Mass Spectroscopic Analysis. Target audience: Bioequivalency centers, QC.

Feb. 2009

The state of the Art laboratories of SANA Pharma has been inspected and accredited by JFDA (Jordan Food and Drugs Administration) for Good Laboratory Practice (GLP). This accreditation includes the following activities: