Dear Dave,
I am not in USA and my previous (canning) experience is 15+ years old but i believe that at that time, one had to USA/FDA
register the process sterilisation details in order to legally market the product?. In the case of low-acid products, I can recall using an official publication defining minimum processing conditions for a range of products / can sizes ?
One quite common consequence (at that time) of a lack of knowledge of the kind of data to which Zeeshan is referring was exploding cans before, during or after shipment. (Of course, lack of appropriate sealing procedures is also a major opportunity for disaster). Was (and maybe still is) excellent business for inspection companies though.
I concluded from my interactions in this field that it is remarkably easy to produce shelf-stable products. Especially unstable (and possibly unsafe) ones.

Of course, such issues are typical (and valid IMO) reasons for justification of official control measures to exist.
@Zeeshan, It might be interesting if you could post a typical example of the (safe) current process conditions / validation to which you are seeking further guidance on ? I deduce that you are actually seeking
individual self-assurance of their reliability ? Unfortunately, as you can probably see, a not-inconsiderable knowledge of theoretical food technology is required in addition to appreciating the (safe) compromises required to make the conclusions operationally practical.
Rgds / Charles.C