Latest Publications
In The Press
Praesent lectus leo, convallis id neque nec, ultrices euismod nibh. Sed ac rhoncus quam. Fusce tristique tellus diam, vel porta eros iaculis vitae.
3 Challenging Complexities of Preclinical Toxicology Studies
Each phase of tox screening introduces unique variables [...]
Critical Reasons to Invest in Pharmaceutical Analytical Services
From screening to development to manufacturing, analytical partners [...]
Quality Standards to Consider When Selecting a Sterile CMO
Your manufacturing partner should demonstrate commitments to transparency [...]
Five Crucial Areas of Concern in Any GLP Lyophilization Process
Although lyophilization (freeze-drying) is a costly, time-consuming process, [...]
3 Surprising Areas in Which Solid State Chemistry Is Rapidly Evolving
Active pharmaceutical ingredients (APIs) can take a [...]
4 Key Advantages of Lyophilizing Your Active Pharmaceutical Ingredient
When a drug must be preserved over [...]
6 Critical Features of a Sterile Fill-and-Finish Cleanroom
Sterile drugs are crucial as treatments for [...]
On-Going Research
Praesent lectus leo, convallis id neque nec, ultrices euismod nibh. Sed ac rhoncus quam. Fusce tristique tellus diam, vel porta eros iaculis vitae.
3 Challenging Complexities of Preclinical Toxicology Studies
Each phase of tox screening introduces unique variables into the process, demanding agility and expertise from testing teams. by Susan Thompson, Technical Director at VxP Pharma Once a drug formulation has demonstrated its viability as [...]
Critical Reasons to Invest in Pharmaceutical Analytical Services
From screening to development to manufacturing, analytical partners provide invaluable insights. Traditional pharmaceutical manufacturing has always involved a certain amount of trial and error. Polymorphs and biological molecules are screened as they're detected. Pilot batches [...]
Quality Standards to Consider When Selecting a Sterile CMO
Your manufacturing partner should demonstrate commitments to transparency and consistency, along with awareness of today’s regulatory landscape. The global market for sterile injectables continues to expand at an impressive rate. In 2015, this market was [...]
Five Crucial Areas of Concern in Any GLP Lyophilization Process
Although lyophilization (freeze-drying) is a costly, time-consuming process, it offers a number of major advantages over simpler dosage forms. Tablets and capsules can create problems for patients with nausea or difficulty swallowing; syringes can carry [...]
4 Key Advantages of Lyophilizing Your Active Pharmaceutical Ingredient
When a drug must be preserved over a long period under uncontrolled conditions, pharma developers turn to lyophilization. By removing residual moisture without applying intense heat, safeguards active pharmaceutical ingredients (APIs) in the five [...]
6 Critical Features of a Sterile Fill-and-Finish Cleanroom
Sterile drugs are crucial as treatments for patients with compromised immune systems. However, the manufacture of sterile drugs demands extraordinary attention to detail, not only in terms of equipment and processes, but in the [...]
Discover The Future
We are a multi-disciplinary laboratory committed to focussed and efficient drug discovery