Microbial Limit Testing

The primary goal of microbial limit testing is to determine the microbial content within pharmaceutical samples and assess whether it falls within acceptable limits defined by regulatory agencies.Key Responsibilities:Determine microbial content in various sample types, including raw materials, intermediates, finished products, and environmental samplesApply...

Initially, microorganisms present in the samples are isolated and cultured using appropriate media and incubation conditions to obtain pure cultures.Subsequently, a combination of techniques such as microscopic examination and biochemical tests are applied for accurate identification inside of our dedicated microbiological labs.Automated systems such as our...

Job Title: Microbial Identification SpecialistAbout the Role:We are seeking a highly skilled Microbial Identification Specialist to join our team. As a key member of our laboratory, you will be responsible for identifying and characterizing microorganisms from various samples using advanced techniques.Key Responsibilities:Isolate and culture microorganisms...

GPT confirms the suitability of culture media for various applications, including environmental monitoring, sterility testing, and microbial limits tests.By regularly performing GPT, companies can:Verify Media QualityEnsure that each batch of culture media can support the growth of target microorganisms.Maintain ComplianceAdhere to regulatory standards set...

At Tentamus Pharma UK, we offer comprehensive Antimicrobial Effectiveness Testing (AET) services tailored to meet the unique needs of pharmaceutical companies.Our AET services include:Selection of Relevant MicroorganismsBased on product type and intended use, we select appropriate microorganisms for testing.Preparation of Test SamplesWe prepare and inoculate...

We evaluate the effectiveness of antimicrobial preservatives in multi-dose pharmaceutical products, following pharmacopoeial methods (e.g., Ph. Eur., USP).Microbiological analysis of pharmaceutical-grade water, including purified water and water for injection (WFI), to comply with regulatory standards.Accurate species-level identification of bacteria, fungi,...

The primary objective of water testing in pharmaceutical manufacturing is to ensure the purity and quality of the water used.Key Responsibilities:Verify water suitability according to Ph. Eur. 0008 standardsRegularly conduct microbiological monitoring to detect and quantify microbial contaminants in waterDetect and quantify bacterial endotoxinsMonitor...

The purity of water used in pharmaceutical manufacturing, whether as an excipient or during analysis, is crucial for maintaining product quality and safety.Confirming water suitability according to Ph. Eur.0008 standards involves thorough testing for various contaminants and properties.Microbiological MonitoringRegular microbiological monitoring is vital to...

Role Summary:We are seeking a professional to confirm the suitability of culture media for various applications. This role involves verifying media quality, ensuring reliable results, and maintaining compliance with regulatory standards.The successful candidate will possess expertise in microbiology and experience in conducting sterility testing, microbial...

During raw materials testing, various aspects are assessed to guarantee quality and safety:IdentityConfirming the correct material is being used.PotencyDetermining the strength or concentration of active ingredients.PurityEnsuring the absence of impurities or contaminants.Physical PropertiesAssessing characteristics like particle size, density, and...