The Strength, Weaknesses, Opportunities, and Threats (SWOT) Analysis of the Establishment of the University of the Philippines Pharmaceutical Science Service Laboratory (UPPSSL) delves into the critical role of pharmaceutical research and service laboratories in advancing drug development, ensuring patient safety, and fostering healthcare innovation. Through a meticulous examination encompassing a literature review, SWOT analysis and Key Informant Interviews (KII), this study evaluates the internal strengths and weaknesses of proposed services such as Product Development, Pharmacokinetic Studies, Therapeutic Drug Monitoring, and Biowaiver Studies. By aligning these services with market demands and regulatory standards, the UPPSSL aims to become a pivotal player in the pharmaceutical research landscape. The validation process through KII ensures that strategic decisions are informed by stakeholder perspectives, enhancing the laboratory's operational efficiency and contribution to the industry.

After The 6th Party Congress, Vietnam pharmaceutical industry prospered, especially in 1990s. Pharmaceutical industry was rising; drug market in Vietnam became eventful and plentiful, responded more and more effectively for the healthcare needs of people. The author mentioned situations of pharmaceutical production and trade in Vietnam during 1996-2002 period: kinds of pharmaceutical companies, situation of drug use, situation of production and trade of Vietnamese pharmaceutical companies and ensuring drug quality
Drug Industry ; Pharmaceutical Preparations

Objects: labour force capital and labour market in some pharmaceutical manufacturing enterprises during years of 1991-1994. Methods: efficacy of working, labour cost, studying and building a period of business, manufacture. High evaluation on needs of human resource, who were trained to become enough standard for moral and talent in arranged sites and close technical process.
Pharmaceutical Preparations ; Drug Industry

Overtaking and coming to meet are a challenge to the Vietnamese pharmacentical industry on the road of integration. A large system such as Vietnam’s pharmaceutical system can cover various smaller system existing in diverse periods of development. Therefore overtaking and coming to meet is a challenge to Vietnam’s pharmacentical industry on the road of international integration. In our country, apart from the slogan of “overtaking the developed countries” there is an other slogan of “coming to meet”. Coming to meet the level of some leading branches of technology is an essential task, needing the concrete and strick management of MOH for developing the pharmacentical system by the years 2005, 2010…; assuring its important position in our national economy
Drug Industry ; Vietnam ; Pharmaceutical Preparations

Process validation is strictly required in good manufacturing practice. For doing so, Shewhart charts can be used effectively. In this work, two types of Shewhart charts including X-bar chart and R chart were applied to validate the production processes of Rantitidin tablets and Tryotricin lozenges. By using six rules of evaluation, the statistical process control of the mean tablet weights were clearly shown
Pharmaceutical Preparations ; Tablets ; Drug Industry

The objectives of prospective process validation are to evaluate the key variables and their operational ranges and to predict the "worst cases" for each investigated variable. The targets of formulation design and optimization are to establish the quantitative relationships between input variables (ingredients/ processing conditions) and output variables (product properties). There are some intersectional ideas between validation and optimization as input-output relationships, quantifiable and predictable behaviours of input and output variables, constraints of independent and dependent variables, etc. The formulation design and optimization for paracetamol tablets, in combination with process prospective validation, using the optimization and what if prediction performed by INForm v3.0 as a frame work, was successfully done to (a) determine the critical variables as well as to estimate their optimized values, (b) to investigate the variable limits as well as to predict some worst cases
Pharmaceutical Preparations ; Formularies ; Drug Industry

Validation is an essential requirement of GMP in current World. Requirement of GMP Validation of ASEAN: (1) Validation on manufacturing process. (2) Validation on quantitative method. 3. Validation on equipment. 4. Validation on hygienic standard and hygienic procedures. Results: (1) Guarantee manufacture to have a products, which respond regulated quality. (2) Respond regulated requirement of decree
Jurisprudence ; Pharmaceutical Preparations ; Drug Industry

OBJECTIVETo optimize the objective technical parameter for direct processing technology of fresh-cut for Paeonia Radix Alba.

METHODPeoniflorin and TGP were employed as the indexes of quality evaluation. Combining with the appearance of the slices, we investigated the influence of slice degree and thickness, drying temperature, drying time, drying method and other factors on the quality control of Paeonia Radix Alba slices. Furthermore, the key fresh-cut technology operating procedures parameter for Paeonia Radix Alba in Bozhou was established based on the semi-works production.

RESULTIt established tentatively the method for fresh-out and fresh-out after boiled of Paeonia Radix Alba as that selected fresh or beiled Paeonia Radix Alba, then divided them from different grades and put them into a roller to crash off the skin, cleaned and then dried them 9 h at 60 degrees C (water content 28% - 32%), and then moistened 2-3 h after spraying moderate water. Cut them into 1.5-2 mm decoction pieces and dried them at 60 degrees C, cooled, and sealed them in a package.

CONCLUSIONThe industrialization of processing decoction pieces with freshly cut Paeonia Radix Alba is stable shortens processing time, avoids effectively sulfur fumigation and infiltrating and soften, and keep high quality of production.

Deal with real situation of now Vietnam’s pharmaceutical industry and get to GMP factories quantity, foreign investment projects in pharmaceutical domain, pharmaceutical market and produce proceeds in home from 1995 to 2002. Immediately challenges as complicated illness model, in home of pharmaceutical industry depend on about not significant make drug material, investment funds of foreign in pharmaceutical industry, limited health budget and paying ability for health service and drug is very scanty. Chances and advantages to develop pharmaceutical industry to 2010.
Drug Industry ; Drug Utilization ; Pharmaceutical Preparations

The strategy of pharmaceutical industry for 2002 - 2010 period” that was approved by Primer Minister mentioned to the need of build-up priority policies for businesses which have invested to researching, developing and innovating the pharmaceutical technology, encouraging the use of generic drug and medications made in Vietnam. An authority for nationwide regulating the medication price should be established as soon as possible. The Drug Management Administration should play more active role as a bridge between manufacturers, prescribers and patients. The national manufacturers should consider employing international experts to approach and learn their experiences and management models as well as acquaint with regulations in GMP. Out-state drug quality surveillance should be available
Adjuvants, Pharmaceutic ; Drug Industry ; Technology, Pharmaceutical