 A CUBE TIC (AJA) Biopharma Limited has obtained an AJA Certificate. AJA Europe, A Cube TIC represents the most recent evolution of our company. In 2022, they changed their name to A Cube TIC, an organization that provides a wide range of services for the quality, safety, sustainability, and performance of systems, products, and people. As a leader in Analysis, Assessment, and Assurance, they support companies of all dimensions, international groups, and institutions that want to improve their operational performance and corporate image.

 The United Kingdom Accreditation Service (UKAS) Biopharma Limited is a UKAS (United Kingdom Accreditation Service) certified company, the national accreditation body for the United Kingdom, appointed by the government to assess organizations that provide certification, testing, inspection, and calibration services.  The United Kingdom Accreditation Service (UKAS) Biopharma Limited is a UKAS (United Kingdom Accreditation Service) certified company, the national accreditation body for the United Kingdom, appointed by the government to assess organizations that provide certification, testing, inspection, and calibration services.  The United Kingdom Accreditation Service (UKAS) Biopharma Limited is a UKAS (United Kingdom Accreditation Service) certified company, the national accreditation body for the United Kingdom, appointed by the government to assess organizations that provide certification, testing, inspection, and calibration services.

 Quality Assured Company ISO 9001:2015 Biopharma Limited is an ISO 9001: 2015 certified company. It is defined as the international standard that specifies requirements for a quality management system (QMS). Organizations use the standard to demonstrate the ability to consistently provide products and services that meet customer and regulatory requirements.

Biopharma was rewarded with this award in 2019. This award aims to recognize "TIGERS" in marketing, branding, CSR & social innovation, education & academics across leadership levels in individuals and organizations that believe that excellence is infinite and perfection has no limit. Targets are milestones, not the end of the journey. The Golden Globe Tigers Awards are multifunctional, multidiscipline industry across segments and industry-focused. Winning the Golden Globe Tigers award is the highest recognition individuals and organizations can aim to achieve because they believe that perfection has no limit...

The CGMP (Current Good Manufacturing Practice) regulations for drugs contain minimum requirements for the methods, facilities, and controls used in the manufacturing, processing, and packing of a drug product. The rules make sure that a product is safe for use and that it has the ingredients and strength it claims to have Good manufacturing practices (GMPs) help to ensure the consistent quality and safety of products by focusing attention on five key elements, which are often referred to as the 5 P's of GMP—people, premises, processes, products, and procedures (or paperwork). GMP Accreditations: Benchmarked to the global regulatory standards, Biopharma Limited's manufacturing facilities have been audited and approved by the following countries' Drug Regulatory Authorities:  Pharmacy & Poisons Board (PPB), Kenya The Pharmacy and Poisons Board is the Drug Regulatory Authority established under the Pharmacy and Poisons Act, Chapter 244 of the Laws of Kenya. The Board regulates the Practice of Pharmacy and the Manufacture and Trade of Drugs and Poisons.  National Agency for Food and Drug Administration and Control (NAFDAC), Nigeria, The National Agency for Food and Drug Administration and Control (NAFDAC) was established by Decree No. 15 of 1993 as amended by Decree No. 19 of 1999 and now the National Agency for Food and Drug Administration and Control Act Cap N1 Laws of the Federation of Nigeria (LFN) 2004 to regulate and control the manufacture, importation, exportation, distribution, advertisement, sale and use of Food, Drugs, Cosmetics, Medical Devices, Packaged Water, Chemicals and Detergents (collectively known as regulated products). The agency was officially established in October 1992.  Pharmacy and Drug Management (DPM) of Cote d'Ivoire, Ivory Coast According to the WHO pharmaceutical country profile, the Pharmacy and Drug Management (DPM) of Cote d' Ivoire performs the following regulatory functions: market authorization, pharmacovigilance, clinical trials, market and quality control, inspection, licensing, promotion and advertisement of medicines and import control.  The Directorate of Pharmacy and Medicine (DPM) Democratic Republic of Congo (DRC) The Directorate of Pharmacy and Medicine of the Republic of Congo (la Direction de la Pharmacie et du Médicament de la République du Congo) is responsible for pharmaceutical dispensing and drug manufacturing in Congo (DPM CONGO, 2020). There is no indication of using an integrated Regulatory Information Management System (I-RIMS).

GOLDEN EUROPE AWARD FOR QUALITY Biopharma Limited has been awarded the “GOLDEN EUROPE AWARD FOR QUALITY” in recognition of its commitment to the Quality and Excellence of its Services on 22nd October 2018.

Biopharma Limited has been awarded Asia’s Greatest Brand 2018 in Singapore by Asia One (Research by United Research Services Asian Business & Social Forum Singapore2019) in the category of Pharmaceuticals.