Raab Scientific Solutions took center stage at the Health Asia Expo Karachi 2022, where the company showcased its expertise and cutting-edge solutions in the healthcare sector. The Raab Scientific Solutions stall at the expo served as a hub for healthcare professionals,…
Pakistan Association of Pathologists (PAP) Conference 2023
Raab Scientific Solutions was a distinguished participant at the Pakistan Association of Pathologists (PAP) Conference 2023, where the company’s stall stood as a focal point for pathologists, laboratory professionals, and medical experts. The stall served as an interactive platform, showcasing Raab…
Seminar At PKLI Lahore
Raab Scientific Solutions took a proactive step in knowledge dissemination by conducting a seminar at the Pakistan Kidney and Liver Institute (PKLI) in Lahore. The seminar served as a platform for sharing expertise, insights, and the latest advancements in scientific solutions…
Pharma Asia Expo Karachi 2023
Raab Scientific Solutions showcased its innovative products and services at the Pharma Asia Expo Karachi 2023 exhibition. The event, held in Karachi, provided a platform for the company to engage with industry leaders, professionals, and potential clients in the pharmaceutical sector….
An In-vitro Comparison between the Branded Xeloda® 500Mg and its Intended Copy Capeda 500 Mg
Generic drug usually means a drug that has the same qualitative and quantitative composition of the active ingredient and the same pharmaceutical form as the reference branded drug, and whose bioavailability with the reference drug has been demonstrated by an appropriate…
Process Validation for Aceclofenac 100mg and Paracetamol 500mg Tablets
According to Indian GMP validation study is essential part of GMP. Those required to be done as per predetermined protocols. Prospective process validation1, 2 is carried out during the development stage by means of risk analysis of the production process which…
Studies In Process Validation For IBUPROFEN 200mg & ETHOCARBAMOL 500mg Caplets Dosage Formulation
According to Indian GMP validation study is essential part of GMP. Those required to be done as per predetermined protocols. Prospective process validation1, 2is carried out during the development stage by means of risk analysis of the production process which is…
Formulation and in vitro evaluation of theophylline-Eudragit®sustained-release tablets
In the last few years controlled release dosage forms have made significant progress in terms of clinical efficacy and patient compliance. The objective of designing a controlled release system is to deliver drug at a rate necessary to achieve and maintain…
Enhanced Data Integrity
RigakuSync is an advanced, optionally automated companion software application that allows the Rigaku Progeny 1064 nm handheld Raman analyzer to securelytransfer scan data from a device to a PC. The RigakuSync application has an option to allow automatic “blind” backup of…
Progeny Handheld 1064nm Raman Trade-In Program
Polymorphs are chemicals with the same atomic components but the physical arrangement of the molecules differ. The differences in their structures cause polymorphs to behave differently—and within the pharmaceutical industry—this means bioavailability changes. It is important to differentiate polymorph types in…