Search Results - "Current good manufacturing practices"

Protein Therapeutic Quality Control Using Multi-Attribute Method (MAM): Challenges and Current Practice in cGMP Environments.

Authors: Hao, Zhiqi Yu, Christopher Bathke, Anja et al.

Source: Pharmaceuticals (14248247). Sep2026, Vol. 19 Issue 9, p1444. 20p.

Strengthening vocational student entrepreneurship through food product standardization at SMK Islam Anharul Ulum Blitar.

Alternate Title: Penguatan kewirausahaan siswa SMK melalui standardisasi produk pangan di SMK Islam Anharul Ulum Blitar.

Authors: Mahmudah, Nur Aini Utama, Adiguna Sasama Wahyu Putra, Aditya Wirawantoro et al.

Source: Journal of Community Service & Empowerment. Aug2026, Vol. 7 Issue 2, p586-594. 9p.

Engineering Allogeneic FE002-Cart Chondroprogenitor Spheroids for Large Knee Chondral Defects: Investigating Microenvironmental Cues for Functional Control, GMP Formulation, and Logistical Viability.

Authors: Applegate, Lee Ann Hadjab, Farid Jaccoud, Sandra et al.

Source: Pharmaceutics. Aug2026, Vol. 18 Issue 8, p1032. 48p.

Next-Generation Nanocarrier Platforms for RNA Vaccines: Advances in Formulation, Stability Engineering, and Translational Manufacturing Challenges.

Authors: Fallatah, Mohannad M. Al-Khaldi, Samiyah Alrabiah, Dimah K. et al.

Source: Pharmaceutics. Aug2026, Vol. 18 Issue 8, p909. 40p.

Enhancing Food Safety Training for Small-Scale Processors: An Interactive Digital GMP Educational Module.

Authors: Cezarotto, Matheus Kinchla, Amanda Coleman, Shannon et al.

Source: Food Protection Trends. May/Jun2026, Vol. 46 Issue 3, p232-241. 10p.

Fully GMP-complient radiosynthesis of [¹⁶¹Tb]Tb-PSMA-1 using the miniAiO synthesizer for clinical translation.

Authors: Kryza, David Le Fur, Pierre Badel, Jean Noël et al.

Source: EJNMMI Radiopharmacy & Chemistry. 6/23/2026, Vol. 11 Issue 1, p1-15. 15p.

Active Pharmaceutical Ingredients in Medical Cannabis: Manufacturer Profiling, Standardization Challenges, and Technological Compatibility.

Authors: Vyshnevska, Liliia Yaromiy, Maryana Pestun, Iryna et al.

Source: Scientia Pharmaceutica. Jun2026, Vol. 94 Issue 2, p41. 21p.

Good Manufacturing Practice-Derived Human Liver Stem Cell Extracellular Vesicles Attenuate Liver Fibrosis In Vivo.

Authors: Ceccotti, Elena Dimuccio, Veronica Pasquino, Chiara et al.

Source: Cells (2073-4409). Apr2026, Vol. 15 Issue 8, p661. 21p.

Outside in: assessment of microbial composition of the crust of dry-aged beef and its relevance in relation to food business operator practices.

Authors: Savini, Federica Indio, Valentina Prandini, Laura et al.

Source: Italian Journal of Food Safety. 2026, Vol. 15 Issue 2, p1-7. 7p.

An improved fully-automated GMP radiosynthesis of [¹⁸F]fluoro-pivalic acid with solid-phase extraction purification.

Authors: Barnes, Chris Twyman, Frazer Awais, Ramla O. et al.

Source: EJNMMI Radiopharmacy & Chemistry. 3/21/2026, Vol. 11 Issue 1, p1-14. 14p.

Assessment of current good manufacturing practice (cGMP) compliance in pharmaceutical manufacturers in Ethiopia: Cross-sectional descriptive study.

Authors: Adola, Teka Benti Assefa, Desta Ejeta, Fikadu et al.

Source: PLoS ONE. 3/9/2026, Vol. 21 Issue 3, p1-16. 16p.

From laboratory to production: a journey of GMP implementation for controlled ice nucleation in Amgen's manufacturing network.

Authors: Al Bakri, Wisam Ganguly, Arnab Ehrlich, Brigid et al.

Source: AAPS Open. 3/9/2026, Vol. 12 Issue 1, p1-15. 15p.

Knowledge Calibration in Pharmaceutical Training: Asymmetric Bias and the Influence of Adaptive E‐Learning, Expertise and Satisfaction.

Authors: Langendorf, Lasse Nielsen Khalid, Md Saifuddin

Source: International Journal of Training & Development. Aug2026, p1. 18p. 6 Illustrations.

cGMP-compliant high-yield automated production of [¹⁸F]AlF-FAPI-74: optimization of quality control and evaluation of molar dose impact.

Authors: Storms, Ward Celen, Sofie Maes, Justine et al.

Source: EJNMMI Radiopharmacy & Chemistry. 12/14/2025, Vol. 10 Issue 1, p1-23. 23p.

An Evaluation of Manufacturing Premises and Equipment Compliances in Indian Biopharmaceutical Industries - A Questionnaire-based Study.

Authors: DHIMAN, KRITANGNI DADWAL, NAVJEEVAN KUMAR, ARUN

Source: Journal of Environment & Bio-sciences. Dec2025, Vol. 39 Issue 2, p257-261. 5p.

Customer Complaints and Product Recall Procedures in the Indian Biopharmaceutical Industry: Implementing Good Manufacturing Practices.

Authors: DHIMAN, SHREYA DADWAL, NAVJEEVAN

Source: Journal of Environment & Bio-sciences. Dec2025, Vol. 39 Issue 2, p273-276. 4p.

Toward Translation of Cowpea Mosaic Virus Intratumoral Immunotherapy With a Scalable Production Process.

Authors: Opdensteinen, Patrick Affonso de Oliveira, Jessica Fernanda Jung, Seongwon et al.

Source: Plant Biotechnology Journal. Nov2025, Vol. 23 Issue 11, p5013-5031. 19p.

How Regulation 536/2014 Is Changing Academic Research with Therapeutic Radiopharmaceuticals: A Local Experience.

Authors: Di Iorio, Valentina Boschi, Stefano Brugugnoli, Erika et al.

Source: Pharmaceuticals (14248247). Nov2025, Vol. 18 Issue 11, p1709. 17p.

Technological Possibilities of Shaping the Health Safety of Meat Products—Selected Aspects.

Authors: Więk, Adam Modzelewska-Kapituła, Monika

Source: Applied Sciences (2076-3417); Sep2026, Vol. 16 Issue 18, p9369, 43p

FINDING UNITY: Recent revisions to 21 CFR Part 820 aim to harmonize FDA and international regulations.

Authors: Truong, Michael¹

Source: Quality Progress. Sep2025, Vol. 58 Issue 9, p38-45. 8p.

Subjects: Current good manufacturing practices, Quality standards, Standardization, Medical equipment, United States. Food & Drug Administration, Applicable laws, Government agencies