My know-how in medicinal chemistry helped us comprehend the molecular interactions better, which performed an important purpose in generating a good drug.
A repeat of the process validation to deliver an assurance that variations in the method/equipments released in accordance with modify control strategies will not adversely have an effect on process attributes & product excellent.
Then they fall towards the chamber wall and shift downward to re-enter into air stream at the bottom of your chamber. It's a basically two spray application systems These are (1) significant stress airless (two) reduced tension air atomized.
This website page covers most of the interview questions and answers asked for the duration of a technical interview round of high-quality assurance and validation experts.
This means the suitability of possibly a drug substance or drug products for its intended use. This expression includes these kinds of characteristics since the id, strength and purity.
Exclusive safety measures to generally be taken through the operation. For instance the packaging of a moisture delicate pill may perhaps need to be carried out beneath small humidity problems.
“In a single undertaking, we ended up tasked with enhancing the bioavailability of a potential antimalarial drug. The compound showed terrific in vitro action but very poor absorption in vivo.
Also, I’ve leveraged machine learning algorithms within just computational chemistry to website accelerate the entire process of identifying promising compounds.”
Non-devoted machines: Exactly where a similar piece of equipment is utilized for An array of items formulations. The prevent of cross-contamination between merchandise results in being the leading objective in the cleansing validation effort and hard work. Clearly, cleaning non-committed equipment’s represents a more sizeable obstacle to beat.
Away from Specification (OOS) final results are Those people effects, created for the duration of testing that do not adjust to the suitable specification or criteria or With all the described acceptance requirements.
If you could teleport nearly anything you'd like, truly worth two million pounds or fewer, any where you'd like, what would you end up picking and where by would you teleport it?
Element the in-system control program to get operated. This tends to vary with regards to the complexity of your packaging functions.
What story you’ve here heard has stayed along with you and usually disturbs you anytime you think about it?
Last of all, I participated in frequent audits to recognize any parts of likely non-compliance and took speedy corrective motion Anytime vital.”