Despite their numerous benefits, the use of anti-static additives also presents challenges. The choice of additive depends on the specific application and the desired performance characteristics. Additionally, some additives can alter the physical properties of the plastic, including its strength and transparency. Therefore, thorough testing is essential to ensure the selected additive meets both functional and aesthetic requirements without compromising the material's integrity.
Companies involved in the production of pharmaceutical intermediates must adhere to Good Manufacturing Practices (GMP). This involves maintaining detailed records of manufacturing processes, conducting regular quality checks, and ensuring traceability of raw materials and intermediates throughout the production cycle. Compliance with these regulations not only helps in maintaining product quality but also protects the manufacturers from legal and financial liabilities.
Regional and global factors, plus preparations and delayed cold weather, helped ISO New England survive the winter of 2014-15 with fewer operational issues and less extreme prices, the ISO said Friday.